These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
3. Privacy Risks from Genomic Data-Sharing Beacons. Shringarpure SS; Bustamante CD Am J Hum Genet; 2015 Nov; 97(5):631-46. PubMed ID: 26522470 [TBL] [Abstract][Full Text] [Related]
4. Leveraging reads that span multiple single nucleotide polymorphisms for haplotype inference from sequencing data. Yang WY; Hormozdiari F; Wang Z; He D; Pasaniuc B; Eskin E Bioinformatics; 2013 Sep; 29(18):2245-52. PubMed ID: 23825370 [TBL] [Abstract][Full Text] [Related]
5. Inferring rare disease risk variants based on exact probabilities of sharing by multiple affected relatives. Bureau A; Younkin SG; Parker MM; Bailey-Wilson JE; Marazita ML; Murray JC; Mangold E; Albacha-Hejazi H; Beaty TH; Ruczinski I Bioinformatics; 2014 Aug; 30(15):2189-96. PubMed ID: 24740360 [TBL] [Abstract][Full Text] [Related]
6. Family genome browser: visualizing genomes with pedigree information. Juan L; Liu Y; Wang Y; Teng M; Zang T; Wang Y Bioinformatics; 2015 Jul; 31(14):2262-8. PubMed ID: 25788626 [TBL] [Abstract][Full Text] [Related]
7. De novo inference of stratification and local admixture in sequencing studies. Zhang Y BMC Bioinformatics; 2013; 14 Suppl 5(Suppl 5):S17. PubMed ID: 23734678 [TBL] [Abstract][Full Text] [Related]
8. Two molecular measures of relatedness based on haplotype sharing. Edwards D BMC Bioinformatics; 2015 Nov; 16():383. PubMed ID: 26558877 [TBL] [Abstract][Full Text] [Related]
10. HapFABIA: identification of very short segments of identity by descent characterized by rare variants in large sequencing data. Hochreiter S Nucleic Acids Res; 2013 Dec; 41(22):e202. PubMed ID: 24174545 [TBL] [Abstract][Full Text] [Related]
11. A likelihood ratio-based method to predict exact pedigrees for complex families from next-generation sequencing data. Heinrich V; Kamphans T; Mundlos S; Robinson PN; Krawitz PM Bioinformatics; 2017 Jan; 33(1):72-78. PubMed ID: 27565584 [TBL] [Abstract][Full Text] [Related]
13. A haplotype-aware de novo assembly of related individuals using pedigree sequence graph. Garg S; Aach J; Li H; Sebenius I; Durbin R; Church G Bioinformatics; 2020 Apr; 36(8):2385-2392. PubMed ID: 31860070 [TBL] [Abstract][Full Text] [Related]
15. Opportunities and Challenges in Interpreting and Sharing Personal Genomes. Rubin IR; Glusman G Genes (Basel); 2019 Aug; 10(9):. PubMed ID: 31450660 [TBL] [Abstract][Full Text] [Related]
16. Accurate viral population assembly from ultra-deep sequencing data. Mangul S; Wu NC; Mancuso N; Zelikovsky A; Sun R; Eskin E Bioinformatics; 2014 Jun; 30(12):i329-37. PubMed ID: 24932001 [TBL] [Abstract][Full Text] [Related]
17. PRISM: pair-read informed split-read mapping for base-pair level detection of insertion, deletion and structural variants. Jiang Y; Wang Y; Brudno M Bioinformatics; 2012 Oct; 28(20):2576-83. PubMed ID: 22851530 [TBL] [Abstract][Full Text] [Related]
18. Fast and Accurate Shared Segment Detection and Relatedness Estimation in Un-phased Genetic Data via TRUFFLE. Dimitromanolakis A; Paterson AD; Sun L Am J Hum Genet; 2019 Jul; 105(1):78-88. PubMed ID: 31178127 [TBL] [Abstract][Full Text] [Related]