Fact-checked by Grok 2 weeks ago

Identity by descent

Identity by descent (IBD) refers to long, nearly identical genomic segments shared between individuals that have been co-inherited from a recent common ancestor, with limited recombination during meiosis breaking them down over generations.^[1] These segments distinguish true genetic relatedness from mere similarity by state (IBS), where DNA appears identical but may not trace to a shared ancestor.^[2] The concept of IBD traces its roots to early genetic principles, including Mendel's laws of inheritance (1866) and formalizations by researchers like Cotterman (1940) and Malécot (1948), who quantified coancestry through shared ancestral material.^[3] It was further advanced by coalescent theory in the 1980s and molecular marker technologies in the late 20th century, enabling precise mapping of shared haplotypes.^[3] In human genetics, IBD segments typically span several centimorgans (cM) for close relatives—such as ~50% of the genome for full siblings—but shorten exponentially with generational distance due to recombination rates of about 1-2 cM per meiosis.^[3] High variance in segment length arises from stochastic processes like Mendelian segregation and variable recombination hotspots across the genome.^[3] Detection of IBD has evolved with genomic data, from pedigree-based linkage analysis to probabilistic methods like hidden Markov models (HMMs) applied to single nucleotide polymorphism (SNP) arrays and whole-genome sequencing.^[1] Modern tools, such as ancIBD for low-coverage ancient DNA or templated positional Burrows-Wheeler transform for large biobanks, can identify segments as short as 2-8 cM in datasets of millions, even accounting for genotyping errors. Recent advances as of 2025 include biobank-scale methods for multi-individual IBD clusters and applications in modeling recent positive selection.^[1]^[2]^[4]^[5] These advances address computational challenges, allowing IBD inference in diverse populations without prior relatedness assumptions.^[2] IBD plays a central role in applications like estimating degrees of relatedness (up to sixth cousins), inferring demographic histories, and mapping rare disease variants by focusing on shared segments enriched for causal alleles.^[1] In population genetics, it reveals fine-scale migration patterns and admixture, as seen in ancient Eurasian samples linking cultures like Yamnaya and Afanasievo.^[1] Additionally, IBD enhances genomic prediction, adjusts for cryptic relatedness in association studies, and supports genealogical research by quantifying recent ancestry within the last 50 generations.^[2]

Fundamentals

Definition

Identity by descent (IBD) refers to segments of DNA that two or more individuals share because they inherited the same haplotype from a recent common ancestor, with no recombination occurring in the generations between the ancestor and the individuals. These shared segments are contiguous stretches of the genome that remain identical due to direct inheritance, distinguishing them from similarities arising independently through mutation or ancient shared ancestry. In genetic analysis, IBD is typically considered for segments longer than a certain length threshold to indicate recent relatedness, as shorter matches may reflect background similarity rather than descent from a specific ancestor.^[6] The concept of identity by descent was introduced in the 1920s by Sewall Wright in the context of quantitative genetics, where it underpinned his development of inbreeding coefficients and path analysis to model correlations among relatives. Although the explicit term and its formal application to phenotypic probabilities were later refined by researchers like Cotterman in 1940 and Malécot in 1948, Wright's foundational work established IBD as a key tool for understanding genetic similarity in pedigrees. This historical framework laid the groundwork for modern uses in tracing inheritance patterns without relying on observed genotypes alone.^[3] For example, full siblings are expected to share approximately 50% of their autosomal genome IBD on average, reflecting the random segregation of parental chromosomes during meiosis. First cousins, sharing a pair of grandparents, typically share about 12.5% of their genome IBD, as the path of inheritance dilutes the shared material across more generations. These proportions illustrate how IBD quantifies relatedness, with longer average segment lengths indicating closer relationships due to fewer recombination events.^[7]^[8] Unlike chance similarities in unrelated individuals, which occur due to the finite number of possible haplotypes in the population and can mimic relatedness at specific loci, IBD specifically traces to a verifiable common ancestor within recent generations, enabling precise genealogical inferences. This differs from identity by state (IBS), a related measure that captures any genomic similarity regardless of ancestral origin.^[9] Identity by descent (IBD) differs fundamentally from identity by state (IBS) in that IBS refers to alleles or genomic segments that are identical in nucleotide sequence, irrespective of their origin, whereas IBD specifically requires that the shared segments are inherited from a recent common ancestor without intervening recombination in the lineage connecting the individuals.^[10] This distinction is critical because IBS can arise from independent mutations, convergent evolution, or shared ancient ancestry due to population history, while IBD traces direct genealogical inheritance.^[9] In structured populations, where allele frequencies vary systematically across subpopulations due to historical isolation or migration, IBS metrics often overestimate relatedness by capturing signals of distant population-level similarity rather than recent shared ancestry; in contrast, IBD provides a more precise measure of genealogical proximity by focusing on uninterrupted haplotype sharing from a common ancestor.^[9] For instance, individuals from the same admixed population may show high IBS due to common ancestral pools but lack detectable IBD segments if their connection is too remote. IBD segments are further categorized as "recent" or "ancient" based on their length, with longer segments typically indicating more recent common ancestors; segments exceeding 2-5 centimorgans (cM) typically reflect sharing within the past 20-50 generations, as shorter segments are more likely to result from ancient coalescence or detection noise.^[11] This length-based distinction arises because meiotic recombination progressively breaks ancestral haplotypes into smaller blocks over generations, limiting the detectable size of IBD for distant relatives while preserving longer, uninterrupted segments for closer kin.^[1]

Theoretical Foundations

Probability Models

The kinship coefficient, denoted \phi, quantifies the probability that two homologous alleles, randomly sampled one from each of two individuals at a given locus, are identical by descent (IBD) from a recent common ancestor.^[12] This coefficient serves as a foundational measure in pedigree-based genetic analysis, capturing the expected allelic sharing due to shared ancestry.^[12] For example, full siblings have a kinship coefficient of \phi = 1/4, reflecting the 50% chance they inherit the same allele from either parent at a locus, while half-siblings have \phi = 1/8, as they share only one parent.^[13] The inbreeding coefficient, denoted f, extends this concept to a single individual and represents the probability that the two alleles at a locus within that individual are IBD, typically from a common ancestor through related parents.^[12] Specifically, f equals the kinship coefficient between the individual's parents, linking inbreeding directly to parental relatedness via IBD probabilities.^[12] This measure is crucial for assessing risks of homozygous genotypes in offspring of consanguineous matings.^[14] To model IBD probabilities across multiple loci along the genome, Markov chain approaches account for linkage and recombination, treating the IBD state at each position as a stochastic process transitioning based on the recombination rate \rho. In these models, the state at a locus (e.g., number of IBD alleles) transitions to adjacent loci with probability $1 - e^{-\rho d}, where d is the genetic distance in Morgans, reflecting the chance of a recombination event breaking IBD continuity.^[15] Seminal formulations, such as those using Jacquard's nine condensed IBD states for diploid pairs, enable computation of joint multilocus probabilities by propagating state distributions via the chain's transition matrix.^[3] Under these models, the expected proportion of the genome shared IBD between two individuals, denoted \pi, equals $2\phi in diploid organisms, representing the average fraction of alleles expected to be IBD across the entire genome assuming uniform recombination.^[16] This relation holds because \phi averages the probabilities of sharing zero, one, or two alleles IBD (\kappa_0, \kappa_1, \kappa_2) such that \phi = (\kappa_1 + 2\kappa_2)/4, yielding \pi = \kappa_1 + 2\kappa_2 = 2\phi.^[16] These probability models rely on key assumptions, including an infinite sites framework for recombination events along an effectively continuous chromosome and negligible mutation rates within recent generations, ensuring that observed allelic identity implies descent without recurrent changes.^[17] Violations, such as significant mutations, would confound IBD inference by introducing identity by state unrelated to descent.^[17]

Segment Length and Distribution

Under the assumption of no interference in recombination (Haldane's model), the lengths of IBD segments shared between two individuals are exponentially distributed, with the mean length L = \frac{1}{2\rho} Morgans (or equivalently $100 / (2\rho) cM), where \rho represents the expected number of recombinations per Morgan along the lineages connecting the individuals to their common ancestor (typically \rho = g for g generations per lineage).^[18] This distribution arises because the positions of recombination events along the genome follow a Poisson process, such that the distance to the nearest recombination event on either side of the shared segment is exponentially distributed with rate $2\rho.^[19] Genome-wide, the expected number of IBD segments between relatives depends on the pedigree relationship and recombination rate; for example, full siblings are expected to share approximately 93 segments across the 22 autosomes.^[20] This accounts for the finite number of chromosomes and the average segment length, yielding higher numbers of shorter segments for closer relatives and fewer, longer segments for more distant ones. Several factors influence the actual distribution of IBD segment lengths beyond the basic exponential model. Recombination interference, where crossovers inhibit nearby events, deviates the distribution from pure exponentiality by increasing the variance in segment lengths and reducing the frequency of very short segments.^[21] Additionally, recombination rates vary across the genome, with hotspots accelerating breakage and coldspots preserving longer segments, leading to heterogeneous length distributions by chromosomal region.^[19] Theoretical models and simulations predict that IBD segments decay exponentially with generations since the common ancestor, as each additional meiosis introduces recombinations that fragment existing segments. For instance, segments from ancestors 10–20 generations ago average 5–10 cM, while those beyond 50 generations often fall below 1 cM and become undetectable with current genotyping resolutions due to errors and incomplete linkage disequilibrium.^[22] These predictions are validated through coalescent simulations incorporating realistic recombination maps, showing a sharp drop in detectable segments for ancient sharing. Recent advances since 2020 have refined these models by incorporating variable effective population sizes (N_e) over time, particularly for inferring ancient IBD in admixed or bottlenecked populations. Such approaches use time-series genomic data to model how fluctuating N_e alters coalescence rates and thus the length spectrum of IBD segments, enabling more accurate reconstruction of demographic histories from low-coverage ancient DNA.^[23]

Applications

Genetic Mapping and Disease Association

Identity by descent (IBD) mapping leverages the principle that affected relatives are more likely to share longer IBD segments around causal loci due to genetic linkage, as these segments are co-inherited with the disease allele and protected from recombination.^[24] This approach identifies genomic regions where excess IBD sharing among affected individuals exceeds expectations under random inheritance, thereby localizing potential disease-causing variants.^[25] In family-based studies, linkage disequilibrium within pedigrees amplifies this signal, enabling the detection of rare variants that may be challenging to identify through population-level association alone.^[26] Fine-mapping using autozygosity, a form of homozygous IBD, is particularly effective for recessive diseases in consanguineous populations, where extended runs of homozygosity (ROH) often encompass the causal locus due to inheritance from a recent common ancestor.^[27] In such families, affected individuals exhibit longer autozygous segments surrounding the disease gene compared to unaffected relatives, allowing researchers to narrow down candidate regions through genome-wide scans for ROH.^[28] This method has successfully mapped numerous Mendelian disorders by prioritizing variants within these homozygous blocks, reducing the search space from millions to thousands of base pairs.^[29] A historical example of IBD-based mapping is the localization of the cystic fibrosis gene in the 1980s, where linkage analysis in extended pedigrees revealed co-segregation of the disease with polymorphic DNA markers on chromosome 7, relying on observed IBD sharing among affected siblings and cousins.^[30] This effort, involving over 100 families, achieved a lod score exceeding 10 for linkage, pinpointing the CFTR locus and facilitating its eventual cloning in 1989.^[31] IBD segments integrate with genome-wide association studies (GWAS) by refining association signals through the identification of shared haplotypes that harbor rare causal variants, effectively filtering spurious associations and highlighting protected segments less prone to recombination.^[32] In large cohorts, IBD mapping complements GWAS by detecting allelic heterogeneity, where multiple rare variants within an IBD-protected haplotype contribute to disease risk, thus enhancing resolution beyond common variant signals.^[26] Despite its strengths, IBD mapping has reduced power in outbred populations due to shorter and sparser IBD segments from distant ancestry, limiting detection of subtle sharing patterns without extensive sample sizes.^[33] Recent advances since 2023, however, have overcome these challenges using large biobanks like the UK Biobank, where efficient algorithms detect multi-individual IBD sharing to identify rare variant associations in hundreds of thousands of unrelated individuals, boosting power for complex traits.^[34]

Population Genetics and Ancestry Inference

In population genetics, identity by descent (IBD) segments serve as powerful indicators for estimating the timing of admixture events, where the length of shared segments inversely correlates with the time since mixing occurred. Longer IBD tracts, typically spanning several centimorgans, signal more recent admixture, as recombination has had less opportunity to erode them over generations. For instance, in African-European admixed populations such as African Americans, analyses of IBD segment lengths have dated primary admixture events to approximately 6–10 generations ago, reflecting historical gene flow during the transatlantic slave trade. This approach leverages the exponential decay of segment lengths under recombination, enabling precise reconstruction of demographic histories in admixed groups.^[35]^[8]^[36] IBD patterns also facilitate the detection of recent positive selection by identifying localized excesses of long haplotype segments around selected loci, where advantageous alleles hitchhike with reduced diversity. Under models of selective sweeps, the distribution of IBD lengths deviates from neutral expectations, with longer segments accumulating near the target site due to suppressed recombination. A 2024 study applied this framework to the lactase persistence locus (LCT), revealing strong selection signals in European populations, with elevated long IBD sharing consistent with adaptive pressures during historical famines that favored dairy consumption.^[37] Such methods outperform traditional site frequency spectrum analyses for events within the last 100 generations, providing robust evidence for adaptive evolution without requiring phased haplotypes. For inferring fine-scale population structure, IBD networks—graphs constructed from pairwise sharing—cluster individuals based on recent common ancestry, illuminating subtle migration patterns and isolation. By embedding genomes in these networks, researchers can delineate substructures within broader groups, such as post-colonial migrations in North America, where IBD connections trace European settler movements and admixture with Indigenous populations over the past 200–300 years. This clustering reveals gene flow barriers and historical bottlenecks at resolutions finer than principal component analysis, aiding in the reconstruction of regional demographic histories.^[38]^[39] Applications to ancient DNA extend IBD analysis to trace deep ancestry, quantifying shared segments between modern and archaic genomes to map introgression events. Short IBD tracts in non-African populations, for example, delineate Neanderthal introgression limits, with total archaic ancestry averaging 1–2% but concentrated in specific genomic regions due to purifying selection against deleterious variants. Recent tools like ancIBD enable reliable detection in low-coverage ancient samples, facilitating studies of migration and admixture, such as Neanderthal gene flow into early modern Europeans dated to 45,000–50,000 years ago. These insights highlight how archaic IBD contributes to modern trait variation while constraining the extent of viable introgressed material.^[40]^[41]^[1] Recent advances from 2023 to 2025 have harnessed large-scale IBD in biobanks, such as the UK Biobank, to uncover cryptic relatedness and population bottlenecks at unprecedented scales. Methods like multi-individual IBD clustering identify hidden pedigrees spanning thousands of samples, revealing unanticipated relatedness that biases association studies and informs founder effects in isolated groups.^[42] In parallel, time-series IBD analyses from biobank cohorts estimate effective population size trajectories, detecting bottlenecks like those in Ashkenazi Jewish populations through excesses of short segments indicative of reduced diversity. These biobank-driven insights, processing millions of segments efficiently, have transformed ancestry inference by integrating IBD with electronic health records to probe evolutionary pressures on disease risk. As of November 2025, ongoing studies continue to refine these methods for deeper demographic insights.^[43]

Relationship and Pedigree Analysis

Identity by descent (IBD) sharing is a key tool for estimating degrees of relatedness between individuals, as the total length of shared IBD segments, measured in centimorgans (cM), correlates with the expected proportion of genome inherited from a common ancestor. For instance, parent-child pairs typically share approximately 3,485 cM (range: 2,376–3,720 cM), reflecting the transmission of one full haplotype set, while full siblings share about 2,613 cM (range: 1,613–3,488 cM) due to recombination in both parental haplotypes. These averages enable probabilistic assignment of relationships, with lower totals indicating more distant kinship, such as 866 cM (range: 396–1,397 cM) for first cousins.^[44] Phasing of genotypes into haplotypes enhances IBD analysis by revealing whether shared segments occur on one (IBD1) or both (IBD2) homologous chromosomes, which is crucial for distinguishing full from half-siblings. Full siblings often share substantial IBD2 regions, averaging half their genome in single-haplotype IBD and one-quarter in double-haplotype IBD, as both inherit from the same two parents. In contrast, half-siblings share only IBD1 segments from one shared parent, lacking the IBD2 pattern, allowing reliable differentiation even when total shared lengths overlap.^[1] Pedigree reconstruction leverages pairwise IBD sharing to build graphical models of family relationships, particularly useful in adoptee studies where parental identities are unknown. Algorithms infer connections by clustering individuals based on shared segment lengths and patterns, constructing multi-generational trees up to six generations deep with high accuracy in outbreeding scenarios. For example, in adoptee cases, IBD matches from consumer databases can identify biological parents and siblings by triangulating shared segments across multiple relatives, enabling de novo pedigree assembly without prior records.^[45] In forensic applications, IBD analysis supports DNA kinship testing for human identification, such as in disaster victim recovery or missing persons cases, by quantifying shared segments to confirm or refute hypothesized relationships. Tools like KinSNP use dense SNP data to measure IBD for precise kinship degree estimation, outperforming traditional marker-based methods in complex scenarios like distant relatives or degraded samples. This approach has been validated for investigative genetic genealogy, aiding law enforcement in building family trees from crime scene DNA.^[46] Challenges in IBD-based pedigree analysis include handling low-coverage data, common in ancient DNA, where short or erroneous segments complicate detection. Recent improvements, such as the ancIBD method (2023) and READv2 (2024), employ hidden Markov models and genotype imputation to robustly identify IBD in low-coverage ancient genomes, enabling accurate kinship inference in pedigrees spanning millennia, as demonstrated in Neolithic and Bronze Age studies. These advances mitigate false positives from contamination or fragmentation, extending applications to historical populations.^[1]^[47]

Detection Methods

Algorithmic Approaches

Hidden Markov model (HMM)-based methods model the genome as a sequence of hidden states representing IBD and non-IBD regions, capturing transitions driven by recombination events along chromosomes. These approaches estimate the probability of state changes at each marker, using forward-backward algorithms to compute posterior probabilities of IBD and Viterbi decoding to identify segment boundaries. A seminal implementation, fastIBD, applies an HMM to phased haplotypes, searching for consecutive markers sharing identical hidden states to detect short IBD tracts with high power, achieving detection rates of over 60% for segments as small as 0.2 cM in high-coverage data.^[48] Haplotype comparison techniques identify IBD by directly aligning phased haplotypes between individuals, seeking exact or near-exact matches above specified thresholds to distinguish recent descent from background similarity. These methods typically use a seed-and-extend strategy: short identical segments (seeds) are identified via hashing, then extended bidirectionally while allowing limited mismatches to account for genotyping errors, with final segments filtered by length (e.g., >3 cM) and mismatch rate (e.g., <1 per 50 markers). The GERMLINE algorithm exemplifies this, efficiently scanning large cohorts by building hash tables of haplotype segments and extending matches, enabling genome-wide analysis in populations of thousands while prioritizing longer, more reliable IBD evidence.^[49] Window-based scanning methods divide the genome into overlapping windows to compute identity-by-state (IBS) scores, which measure allele sharing, and apply IBD-specific filters such as exponential decay in sharing probability to refine candidates into true descent segments. In this approach, IBS is tallied across fixed window sizes (e.g., 50-100 SNPs), and potential IBD regions are scored based on elevated sharing relative to expected background levels, often combined with local recombination rates to estimate segment confidence. Refined IBD integrates windowed IBS computation with HMM refinement, boosting accuracy by modeling IBS under non-IBD states and reporting segments with low false-positive rates, particularly for intermediate-length tracts. Recent algorithmic advancements address genotyping errors and low-coverage data through iterative phasing and imputation, enhancing robustness for challenging datasets like ancient DNA. These methods incorporate probabilistic genotype calls from imputation tools (e.g., Beagle) into HMM emission probabilities, allowing detection despite missing data or sequencing noise, and use multi-round phasing to resolve ambiguities in haplotype reconstruction. For instance, ancIBD employs an HMM tailored for ancient genomes, imputing low-coverage variants and achieving balanced precision and recall in regimes below 0.5× coverage, where traditional methods fail.^[1] Evaluation of these algorithms commonly uses precision (fraction of reported segments that are true IBD) and recall (fraction of true segments detected), with benchmarks on simulated and real pedigrees showing >90% precision and recall for segments longer than 5 cM across methods like RaPID, TPBWT, and Refined IBD, though performance drops for shorter tracts due to recombination fragmentation.^[50]

Software Tools

GERMLINE, introduced in 2009, is a foundational tool for detecting long identity-by-descent (IBD) segments between pairs of individuals in large cohorts, employing a seed-and-extend approach that scans for shared haplotypes efficiently across genome-wide data.^[49] Its extensions, such as those integrated into subsequent versions and related methods like FastSMC, enhance performance for population-scale analysis by improving speed and accuracy in identifying recent common ancestry in datasets with thousands of samples.^[8] These tools excel in handling phased genotype data for long segments (>3 cM), making them suitable for mapping hidden relatedness in biobanks.^[51] In the 2010s, IBDseq (2013) advanced detection for short IBD segments and error-prone sequencing data using a hidden Markov model (HMM) on unphased genotypes, estimating genotype error rates and IBD probabilities to robustly identify segments as small as 0.5 cM in whole-genome sequencing.^[52] Complementing this, Refined IBD (2013), also HMM-based, refines segment boundaries in phased data with high precision (>99% accuracy for endpoints), reducing false positives while maintaining computational efficiency for medium-sized cohorts.^[53] Both tools address challenges in noisy data, with IBDseq particularly effective for low-coverage sequences and Refined IBD integrated into broader pipelines for accurate post-phasing refinement.^[54] Recent developments from 2020 onward include hap-IBD (2020), which leverages a compressed positional Burrows-Wheeler transform for rapid detection of IBD segments in large-scale phased data, outperforming predecessors in speed and sensitivity for ultra-long haplotypes in biobank-sized datasets exceeding 100,000 samples.^[55] For low-coverage ancient genomes, clusIBD (2025) enables robust clustering and detection of IBD segments in unphased data with high genotype error rates (>20%), using a probabilistic model to infer relatedness in poor-quality samples like archaeological DNA.^[56] Additionally, the gwid R package (2024) facilitates genome-wide visualization and statistical analysis of IBD data for dichotomous traits, supporting hypothesis testing and plotting of segment distributions via integration with tools like Beagle outputs.^[57] Comparatively, Beagle's integrated IBD detection, via modules like fastIBD and Refined IBD, achieves scalability for millions of samples by combining phasing with HMM-based inference, demonstrating superior runtime (e.g., processing 500,000 samples in hours) and low error rates in benchmarks against GERMLINE and hap-IBD.^[58] Most of these tools are open-source, with GERMLINE available on GitHub, IBDseq and Refined IBD distributed via academic repositories, and recent ones like hap-IBD and gwid on CRAN or BioRxiv-linked codebases, often integrating seamlessly with pipelines such as PLINK for association testing or BCFtools for VCF handling.^[59]^[60]

References

[1]
Accurate detection of identity-by-descent segments in human ...
Dec 20, 2023 · Long DNA segments shared between two individuals, known as identity-by-descent (IBD), reveal recent genealogical connections.
[2]
Current Developments in Detection of Identity-by-Descent Methods ...
Sep 10, 2021 · Identity-by-descent is the shared inheritance of an identical portion of the genome between two individuals (Browning, 2008; Gusev et al., 2008; ...
[3]
Identity by Descent: Variation in Meiosis, Across Genomes ... - NIH
Gene identity by descent (IBD) is a fundamental concept that underlies genetically mediated similarities among relatives.
[4]
An Upper Bound on the Power of DNA to Distinguish Pedigree ...
For example, full siblings are expected to share approximately 50% of their autosomal genome IBD on average: about 25% as IBD2 (both alleles identical by ...
[5]
Current Developments in Detection of Identity-by-Descent Methods ...
Sep 9, 2021 · Identity-by-descent is the shared inheritance of an identical portion of the genome between two individuals (Browning, 2008; Gusev et al., 2008; ...Abstract · Introduction · Governing Evolutionary... · Conclusion
[6]
Inference of Relationships in Population Data Using Identity-by ...
These alleles may be shared identical-by-descent (IBD) in which 0, 1, or 2 alleles are inherited from a recent common ancestor, or they may be identical by ...
[7]
Identity-by-descent analyses for measuring population dynamics ...
Identity-by-descent analyses for measuring population dynamics and selection in recombining pathogens. Lyndal Henden. Lyndal Henden. 1Population Health and ...Missing: coined | Show results with:coined
[8]
A Fast and Simple Method for Detecting Identity-by-Descent ...
Mar 12, 2020 · Segments of IBD resulting from shared ancestry 25 generations ago have an expected length of 2 cM, while the typical 2 cM segment has a ...
[9]
[PDF] CHAPTER 2. GENE IDENTITY BY DESCENT 2.1 Kinship and ...
Together with symmetry and boundary conditions, these equations determine the multiple kinship coefficients on any pedigree, although practical implementation ...Missing: formula | Show results with:formula
[10]
[PDF] Identical by Descent (IBD)
Δ7 is also called the coefficient of fraternity. θij is the kinship coefficient, also called the coefficient of coancestry, and is the probability that for a ...Missing: formula | Show results with:formula
[11]
Estimation of inbreeding and kinship coefficients via latent identity ...
The inbreeding coefficient (denoted by F) of an individual is the probability that two parental alleles sampled at a random locus in the genome are IBD.
[12]
Estimating genome-wide IBD sharing from SNP data via an efficient ...
Jun 1, 2010 · We model the recombination probabilities as P(Sij|Si−1j≠Sij) = 1 − e−l, where l is the genetic distance, in Morgans, between location i and i − ...
[13]
A Genomewide Search Using an Original Pairwise Sampling ...
is a matrix of the proportion of alleles shared IBD estimated from the genotypic data at a point in the genome, 2Φ is a matrix of the expected proportion of ...
[14]
Modeling of Identity-by-Descent Processes Along a Chromosome ...
TWO alleles at a single locus are identical-by-descent (IBD) if they derive from a common ancestor without mutation. The probability for two alleles to be IBD ...
[15]
A fast and accurate method for detection of IBD shared haplotypes in ...
Feb 8, 2017 · We developed a new IBD segment detection program, FISHR (Find IBD Shared Haplotypes Rapidly), in an attempt to accurately detect IBD segments and to better ...
[16]
Length Distributions of Identity by Descent Reveal Fine-Scale ...
For example, expansions that occurred more than 100 generations ago leave a negligible signature when IBD segments between 4 and 5 cM in length are considered ( ...
[17]
[PDF] UC Davis - eScholarship.org
Then, the expected number of IBD segments E[N] can be thought of as the average number of alleles shared between two individuals in a genome with nd+c loci ...
[18]
Conflation of Short Identity-by-Descent Segments Bias Their Inferred ...
Identity-by-descent (IBD) is a fundamental concept in genetics with many applications. In a common definition, two haplotypes are said to share an IBD ...Abstract · Methods · Results
[19]
Haplotype-based inference of recent effective population size in ...
Dec 1, 2023 · Here, we present a new method, called HapNe, that enables flexible inference of recent effective population size fluctuations using IBD or LD ...
[20]
A method for detecting IBD regions simultaneously in multiple ... - NIH
... IBD estimation. We used a recombination rate of 1.3 cM per 1 Mb as estimated by Kong et al. (2002). Power analysis. To evaluate the power and accuracy of the ...
[21]
Identity by Descent Between Distant Relatives: Detection and ...
Sep 17, 2012 · Short segments of identity by descent (IBD) between individuals with no known relationship can be detected using genome-wide single nu- cleotide ...
[22]
Identity-by-Descent Mapping to Detect Rare Variants Conferring ...
'Population-based linkage analysis' (PBLA) or so called identity-by-descent (IBD) mapping is a novel way to detect rare variants in extant GWAS datasets.
[23]
AutozygosityMapper: Identification of disease-mutations in ... - NIH
Apr 30, 2022 · INTRODUCTION. Homozygosity mapping is a common technique to study autosomal recessive disease in consanguineous families.
[24]
Research Techniques Made Simple: Genome-Wide Homozygosity ...
Homozygosity mapping (HM), also known as autozygosity mapping, was originally used to map genes underlying homozygous autosomal recessive Mendelian diseases.Introduction · Methodologies And... · Hm Using Wes/wgs Data
[25]
Autozygome decoded | Genetics in Medicine - Nature
Nov 15, 2010 · Consanguineous unions permit the “reunion” of ancestral chromosomal segments in a pattern referred to as “autozygosity,” which is essentially a special form of ...Mechanism And Digital... · Complex Disorders · Disease Gene Mapping
[26]
Cystic fibrosis locus defined by a genetically linked polymorphic ...
Nov 29, 1985 · A polymorphic DNA marker has been found genetically linked, in a set of 39 human families, to an autosomal recessive gene that causes cystic fibrosis (CF).
[27]
Genetic Dissection of Complex Traits - Science
Medical genetics was revolutionized during the 1980s by the application of genetic mapping to locate the genes responsible for simple Mendelian diseases.
[28]
Fast pairwise IBD association testing in genome-wide ... - NIH
One promising application of IBD mapping is to use discovered IBD segments in the association testing (Purcell et al., 2007). Investigators usually test single ...Missing: refine | Show results with:refine
[29]
Identity-by-Descent Mapping Identifies Major Locus for Serum ...
Dec 13, 2017 · Genotypes used in the linkage analysis (to calculate IBD sharing in the autosomal genome and to assess local IBD) were produced with the ...
[30]
A fast identity-by-descent mapping test for biobank-scale cohorts - NIH
Dec 1, 2023 · We developed FiMAP, an efficient IBD mapping test that can be applied to hundreds of thousands of individuals from biobank-scale cohorts.
[31]
The Lengths of Admixture Tracts - PMC - NIH
We compare the expected distribution of admixture tract lengths under a number of population-genetic models to the distribution predicted by the Wright–Fisher ...
[32]
Genome-wide Ancestry and Demographic History of African ...
Nov 2, 2017 · We observed the highest values of summed IBD segments shared between each pair of African-descendant and African individuals who are ...
[33]
Clustering of 770,000 genomes reveals post-colonial population ...
Feb 7, 2017 · Here we identify very recent fine-scale population structure in North America from a network of over 500 million genetic (identity-by-descent, IBD) connections.
[34]
Population Histories of the United States Revealed through Fine ...
Mar 5, 2020 · The population of the United States is shaped by centuries of migration, isolation, growth, and admixture between ancestors of global origins.
[35]
IBD Sharing between Africans, Neandertals, and Denisovans
Feb 1, 2017 · Neanderthal and Denisova genetic affinities with contemporary humans: introgression versus common ancestral polymorphisms . Gene. 530. : 83.
[36]
Earliest modern human genomes constrain timing of Neanderthal ...
Dec 12, 2024 · Ranis genomes harbour Neanderthal segments that originate from a single admixture event shared ... shared introgression event with Neanderthals.
[37]
Estimating effective population size trajectories from time-series ...
Jan 24, 2025 · Identity-by-descent (IBD) segments are long genomic stretches shared by pairs of individuals that result from recent genealogical connections.
[38]
Detection of distant relatedness in biobanks to identify undiagnosed ...
Aug 29, 2024 · Here, we innovatively leverage IBD segments in a large biobank to investigate a rare variant in KCNE1 that is causal for Long QT syndrome (LQTS) ...
[39]
Law enforcement use of genetic genealogy databases in criminal ...
Feb 8, 2024 · The total amount of DNA shared is expressed in centimorgans (cM) [16], where a higher value means a higher degree of familial closeness (Table ...
[40]
Pedigree reconstruction using identity by descent - PubMed
This article introduces two multi-generational pedigree reconstruction methods: one for inbreeding relationships and one for outbreeding relationships. In ...Missing: adoptee studies
[41]
Analytical validation of the IBD segment-based tool KinSNP® for ...
Abstract. KinSNP® v1.0, a software tool for human identification, has been widely used to measure IBD segment sharing between individuals using dense SNP ...
[42]
READv2: advanced and user-friendly detection of ... - Genome Biology
Aug 12, 2024 · READv2 enables user-friendly, efficient, and nuanced analysis of biological relatedness, facilitating a deeper understanding of past social structures.<|control11|><|separator|>
[43]
A Fast, Powerful Method for Detecting Identity by Descent - PMC - NIH
Feb 11, 2011 · The fastIBD detection method is highly accurate for detecting IBD and yet is sufficiently fast to perform genome-wide analysis in large samples.Missing: paper | Show results with:paper
[44]
Whole population, genome-wide mapping of hidden relatedness - NIH
This rate of change in IBD status along a pair of genomes facilitates computing the expected number of IBD segments genome-wide. Table 1 illustrates these ...
[45]
Open-source benchmarking of IBD segment detection methods for ...
Dec 6, 2022 · FastSMC applies hashing methods to identify IBD segments, then uses a coalescent-based hidden Markov model (HMM) to verify the segments.
[46]
RaPID: ultra-fast, powerful, and accurate detection of segments ...
Jul 25, 2019 · We describe an efficient method, RaPID, for detecting IBD segments in a panel with phased haplotypes. RaPID achieves a time and space complexity linear to the ...
[47]
Detecting identity by descent and estimating genotype error rates in ...
Nov 7, 2013 · The IBDseq method estimates probabilities of genotypes observed with error for each pair of individuals under IBD and non-IBD models. The ratio ...
[48]
Improving the Accuracy and Efficiency of Identity-by-Descent ...
We present Refined IBD, a new method for IBD segment detection. Refined IBD achieves both computational efficiency and highly accurate IBD segment reporting.Missing: refinedIBD software
[49]
Refined IBD - UW Faculty Web Server
Jan 17, 2020 · Refined IBD is a software package that detects identity-by-descent segments in phased genotype data.Missing: algorithm | Show results with:algorithm
[50]
A Fast and Simple Method for Detecting Identity-by-Descent ...
Apr 2, 2020 · Our method, called hap-IBD, combines a compressed representation of haplotype data, the positional Burrows-Wheeler transform, and multi-threaded execution to ...
[51]
clusIBD: Robust Detection of Identity-by-descent (IBD) Segments ...
Mar 15, 2025 · We propose a method, clusIBD, which can robustly detect IBD segments using unphased genetic data with high genotype errors.
[52]
gwid: an R package and Shiny application for Genome-Wide ...
Jul 31, 2024 · Identity-by-descent (IBD) mapping is a powerful approach for investigating the genetic underpinnings of complex diseases. When two haplotypes ...Missing: principle | Show results with:principle
[53]
A fast, powerful method for detecting identity by descent - PubMed
Feb 11, 2011 · FastIBD can be applied to thousands of samples across genome-wide SNP data and is significantly more powerful for finding short tracts of IBD ...Missing: paper | Show results with:paper
[54]
gusevlab/germline - GitHub
GERMLINE is an algorithm to infer long shared segments of Identity by Descent (IBD) between pairs of individuals in a large population.
[55]
IBDseq
Dec 19, 2013 · IBDseq is a software program for detecting segments of identity-by-descent (IBD) and homozygosity-by-descent (HBD) in unphased genetic sequence data.