Literature DB >> 29868720

Comparing complex variants in family trios.

Berke Ç Toptas1,2, Goran Rakocevic1,2, Péter Kómár1,2, Deniz Kural1,2.   

Abstract

Motivation: Several tools exist to count Mendelian violations in family trios by comparing variants at the same genomic positions. This naive variant comparison, however, fails to assess regions where multiple variants need to be examined together, resulting in reduced accuracy of existing Mendelian violation checking tools.
Results: We introduce VBT, a trio concordance analysis tool, which identifies Mendelian violations by approximately solving the 3-way variant matching problem to resolve variant representation differences in family trios. We show that VBT outperforms previous trio comparison methods by accuracy. Availability and implementation: VBT is implemented in C++ and source code is available under GNU GPLv3 license at the following URL: https://github.com/sbg/VBT-TrioAnalysis.git. Supplementary information: Supplementary data are available at Bioinformatics online.

Entities:  

Mesh:

Year:  2018        PMID: 29868720      PMCID: PMC6289131          DOI: 10.1093/bioinformatics/bty443

Source DB:  PubMed          Journal:  Bioinformatics        ISSN: 1367-4803            Impact factor:   6.937


  19 in total

1.  The Genome Analysis Toolkit: a MapReduce framework for analyzing next-generation DNA sequencing data.

Authors:  Aaron McKenna; Matthew Hanna; Eric Banks; Andrey Sivachenko; Kristian Cibulskis; Andrew Kernytsky; Kiran Garimella; David Altshuler; Stacey Gabriel; Mark Daly; Mark A DePristo
Journal:  Genome Res       Date:  2010-07-19       Impact factor: 9.043

2.  Variation in genome-wide mutation rates within and between human families.

Authors:  Donald F Conrad; Jonathan E M Keebler; Mark A DePristo; Sarah J Lindsay; Yujun Zhang; Ferran Casals; Youssef Idaghdour; Chris L Hartl; Carlos Torroja; Kiran V Garimella; Martine Zilversmit; Reed Cartwright; Guy A Rouleau; Mark Daly; Eric A Stone; Matthew E Hurles; Philip Awadalla
Journal:  Nat Genet       Date:  2011-06-12       Impact factor: 38.330

3.  The variant call format and VCFtools.

Authors:  Petr Danecek; Adam Auton; Goncalo Abecasis; Cornelis A Albers; Eric Banks; Mark A DePristo; Robert E Handsaker; Gerton Lunter; Gabor T Marth; Stephen T Sherry; Gilean McVean; Richard Durbin
Journal:  Bioinformatics       Date:  2011-06-07       Impact factor: 6.937

4.  Family-Based Benchmarking of Copy Number Variation Detection Software.

Authors:  Marcel Elie Nutsua; Annegret Fischer; Almut Nebel; Sylvia Hofmann; Stefan Schreiber; Michael Krawczak; Michael Nothnagel
Journal:  PLoS One       Date:  2015-07-21       Impact factor: 3.240

Review 5.  Clinical application of next-generation sequencing for Mendelian diseases.

Authors:  Saumya Shekhar Jamuar; Ene-Choo Tan
Journal:  Hum Genomics       Date:  2015-06-16       Impact factor: 4.639

6.  A global reference for human genetic variation.

Authors:  Adam Auton; Lisa D Brooks; Richard M Durbin; Erik P Garrison; Hyun Min Kang; Jan O Korbel; Jonathan L Marchini; Shane McCarthy; Gil A McVean; Gonçalo R Abecasis
Journal:  Nature       Date:  2015-10-01       Impact factor: 49.962

7.  A framework for the detection of de novo mutations in family-based sequencing data.

Authors:  Laurent C Francioli; Mircea Cretu-Stancu; Kiran V Garimella; Menachem Fromer; Wigard P Kloosterman; Kaitlin E Samocha; Benjamin M Neale; Mark J Daly; Eric Banks; Mark A DePristo; Paul Iw de Bakker
Journal:  Eur J Hum Genet       Date:  2016-11-23       Impact factor: 4.246

8.  geck: trio-based comparative benchmarking of variant calls.

Authors:  Péter Kómár; Deniz Kural
Journal:  Bioinformatics       Date:  2018-10-15       Impact factor: 6.937

9.  Prevalence and architecture of de novo mutations in developmental disorders.

Authors: 
Journal:  Nature       Date:  2017-01-25       Impact factor: 49.962

10.  Rate of de novo mutations and the importance of father's age to disease risk.

Authors:  Augustine Kong; Michael L Frigge; Gisli Masson; Soren Besenbacher; Patrick Sulem; Gisli Magnusson; Sigurjon A Gudjonsson; Asgeir Sigurdsson; Aslaug Jonasdottir; Adalbjorg Jonasdottir; Wendy S W Wong; Gunnar Sigurdsson; G Bragi Walters; Stacy Steinberg; Hannes Helgason; Gudmar Thorleifsson; Daniel F Gudbjartsson; Agnar Helgason; Olafur Th Magnusson; Unnur Thorsteinsdottir; Kari Stefansson
Journal:  Nature       Date:  2012-08-23       Impact factor: 49.962

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  6 in total

Review 1.  Next Generation Sequencing and Bioinformatics Analysis of Family Genetic Inheritance.

Authors:  Aquillah M Kanzi; James Emmanuel San; Benjamin Chimukangara; Eduan Wilkinson; Maryam Fish; Veron Ramsuran; Tulio de Oliveira
Journal:  Front Genet       Date:  2020-10-23       Impact factor: 4.599

2.  Performance assessment of DNA sequencing platforms in the ABRF Next-Generation Sequencing Study.

Authors:  Jonathan Foox; Scott W Tighe; Charles M Nicolet; Justin M Zook; Marta Byrska-Bishop; Wayne E Clarke; Michael M Khayat; Medhat Mahmoud; Phoebe K Laaguiby; Zachary T Herbert; Derek Warner; George S Grills; Jin Jen; Shawn Levy; Jenny Xiang; Alicia Alonso; Xia Zhao; Wenwei Zhang; Fei Teng; Yonggang Zhao; Haorong Lu; Gary P Schroth; Giuseppe Narzisi; William Farmerie; Fritz J Sedlazeck; Don A Baldwin; Christopher E Mason
Journal:  Nat Biotechnol       Date:  2021-09-09       Impact factor: 54.908

3.  E-Pedigrees: a large-scale automatic family pedigree prediction application.

Authors:  Xiayuan Huang; Nicholas Tatonetti; Katie LaRow; Brooke Delgoffee; John Mayer; David Page; Scott J Hebbring
Journal:  Bioinformatics       Date:  2021-06-04       Impact factor: 6.931

4.  geck: trio-based comparative benchmarking of variant calls.

Authors:  Péter Kómár; Deniz Kural
Journal:  Bioinformatics       Date:  2018-10-15       Impact factor: 6.937

5.  An open resource for accurately benchmarking small variant and reference calls.

Authors:  Justin M Zook; Jennifer McDaniel; Nathan D Olson; Justin Wagner; Hemang Parikh; Haynes Heaton; Sean A Irvine; Len Trigg; Rebecca Truty; Cory Y McLean; Francisco M De La Vega; Chunlin Xiao; Stephen Sherry; Marc Salit
Journal:  Nat Biotechnol       Date:  2019-04-01       Impact factor: 54.908

Review 6.  Best practices for variant calling in clinical sequencing.

Authors:  Daniel C Koboldt
Journal:  Genome Med       Date:  2020-10-26       Impact factor: 11.117

  6 in total

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