Literature DB >> 21159622

Using bioinformatics to predict the functional impact of SNVs.

Melissa S Cline1, Rachel Karchin.   

Abstract

MOTIVATION: The past decade has seen the introduction of fast and relatively inexpensive methods to detect genetic variation across the genome and exponential growth in the number of known single nucleotide variants (SNVs). There is increasing interest in bioinformatics approaches to identify variants that are functionally important from millions of candidate variants. Here, we describe the essential components of bioinformatics tools that predict functional SNVs.
RESULTS: Bioinformatics tools have great potential to identify functional SNVs, but the black box nature of many tools can be a pitfall for researchers. Understanding the underlying methods, assumptions and biases of these tools is essential to their intelligent application.

Mesh:

Substances:

Year:  2010        PMID: 21159622      PMCID: PMC3105482          DOI: 10.1093/bioinformatics/btq695

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


  69 in total

Review 1.  Post-translational modifications and their biological functions: proteomic analysis and systematic approaches.

Authors:  Jawon Seo; Kong-Joo Lee
Journal:  J Biochem Mol Biol       Date:  2004-01-31

2.  The International HapMap Project.

Authors: 
Journal:  Nature       Date:  2003-12-18       Impact factor: 49.962

3.  SIFT: Predicting amino acid changes that affect protein function.

Authors:  Pauline C Ng; Steven Henikoff
Journal:  Nucleic Acids Res       Date:  2003-07-01       Impact factor: 16.971

4.  The Swiss-Prot variant page and the ModSNP database: a resource for sequence and structure information on human protein variants.

Authors:  Yum L Yip; Holger Scheib; Alexander V Diemand; Alexandre Gattiker; Livia M Famiglietti; Elisabeth Gasteiger; Amos Bairoch
Journal:  Hum Mutat       Date:  2004-05       Impact factor: 4.878

Review 5.  Prioritizing GWAS results: A review of statistical methods and recommendations for their application.

Authors:  Rita M Cantor; Kenneth Lange; Janet S Sinsheimer
Journal:  Am J Hum Genet       Date:  2010-01       Impact factor: 11.025

6.  Heritable individual-specific and allele-specific chromatin signatures in humans.

Authors:  Ryan McDaniell; Bum-Kyu Lee; Lingyun Song; Zheng Liu; Alan P Boyle; Michael R Erdos; Laura J Scott; Mario A Morken; Katerina S Kucera; Anna Battenhouse; Damian Keefe; Francis S Collins; Huntington F Willard; Jason D Lieb; Terrence S Furey; Gregory E Crawford; Vishwanath R Iyer; Ewan Birney
Journal:  Science       Date:  2010-03-18       Impact factor: 47.728

Review 7.  Bioinformatic tools for identifying disease gene and SNP candidates.

Authors:  Sean D Mooney; Vidhya G Krishnan; Uday S Evani
Journal:  Methods Mol Biol       Date:  2010

8.  Alternative splicing in disease and therapy.

Authors:  Mariano A Garcia-Blanco; Andrew P Baraniak; Erika L Lasda
Journal:  Nat Biotechnol       Date:  2004-05       Impact factor: 54.908

9.  Complete Khoisan and Bantu genomes from southern Africa.

Authors:  Stephan C Schuster; Webb Miller; Aakrosh Ratan; Lynn P Tomsho; Belinda Giardine; Lindsay R Kasson; Robert S Harris; Desiree C Petersen; Fangqing Zhao; Ji Qi; Can Alkan; Jeffrey M Kidd; Yazhou Sun; Daniela I Drautz; Pascal Bouffard; Donna M Muzny; Jeffrey G Reid; Lynne V Nazareth; Qingyu Wang; Richard Burhans; Cathy Riemer; Nicola E Wittekindt; Priya Moorjani; Elizabeth A Tindall; Charles G Danko; Wee Siang Teo; Anne M Buboltz; Zhenhai Zhang; Qianyi Ma; Arno Oosthuysen; Abraham W Steenkamp; Hermann Oostuisen; Philippus Venter; John Gajewski; Yu Zhang; B Franklin Pugh; Kateryna D Makova; Anton Nekrutenko; Elaine R Mardis; Nick Patterson; Tom H Pringle; Francesca Chiaromonte; James C Mullikin; Evan E Eichler; Ross C Hardison; Richard A Gibbs; Timothy T Harkins; Vanessa M Hayes
Journal:  Nature       Date:  2010-02-18       Impact factor: 49.962

10.  Sequence-based feature prediction and annotation of proteins.

Authors:  Agnieszka S Juncker; Lars J Jensen; Andrea Pierleoni; Andreas Bernsel; Michael L Tress; Peer Bork; Gunnar von Heijne; Alfonso Valencia; Christos A Ouzounis; Rita Casadio; Søren Brunak
Journal:  Genome Biol       Date:  2009-02-02       Impact factor: 13.583

View more
  39 in total

Review 1.  Bioinformatics for personal genome interpretation.

Authors:  Emidio Capriotti; Nathan L Nehrt; Maricel G Kann; Yana Bromberg
Journal:  Brief Bioinform       Date:  2012-01-13       Impact factor: 11.622

2.  GenomeRunner: automating genome exploration.

Authors:  Mikhail G Dozmorov; Lukas R Cara; Cory B Giles; Jonathan D Wren
Journal:  Bioinformatics       Date:  2011-12-06       Impact factor: 6.937

3.  Incorporating molecular and functional context into the analysis and prioritization of human variants associated with cancer.

Authors:  Thomas A Peterson; Nathan L Nehrt; Dohwan Park; Maricel G Kann
Journal:  J Am Med Inform Assoc       Date:  2012 Mar-Apr       Impact factor: 4.497

4.  IMHOTEP-a composite score integrating popular tools for predicting the functional consequences of non-synonymous sequence variants.

Authors:  Carolin Knecht; Matthew Mort; Olaf Junge; David N Cooper; Michael Krawczak; Amke Caliebe
Journal:  Nucleic Acids Res       Date:  2017-02-17       Impact factor: 16.971

5.  Human germline and pan-cancer variomes and their distinct functional profiles.

Authors:  Yang Pan; Konstantinos Karagiannis; Haichen Zhang; Hayley Dingerdissen; Amirhossein Shamsaddini; Quan Wan; Vahan Simonyan; Raja Mazumder
Journal:  Nucleic Acids Res       Date:  2014-09-17       Impact factor: 16.971

Review 6.  Tools for Predicting the Functional Impact of Nonsynonymous Genetic Variation.

Authors:  Haiming Tang; Paul D Thomas
Journal:  Genetics       Date:  2016-06       Impact factor: 4.562

7.  A Molecular Evolutionary Reference for the Human Variome.

Authors:  Li Liu; Koichiro Tamura; Maxwell Sanderford; Vanessa E Gray; Sudhir Kumar
Journal:  Mol Biol Evol       Date:  2015-10-13       Impact factor: 16.240

8.  Predicting pathogenicity of missense variants with weakly supervised regression.

Authors:  Yue Cao; Yuanfei Sun; Mostafa Karimi; Haoran Chen; Oluwaseyi Moronfoye; Yang Shen
Journal:  Hum Mutat       Date:  2019-08-07       Impact factor: 4.878

9.  Missense variants in CFTR nucleotide-binding domains predict quantitative phenotypes associated with cystic fibrosis disease severity.

Authors:  David L Masica; Patrick R Sosnay; Karen S Raraigh; Garry R Cutting; Rachel Karchin
Journal:  Hum Mol Genet       Date:  2014-12-08       Impact factor: 6.150

Review 10.  Genotype to phenotype via network analysis.

Authors:  Hannah Carter; Matan Hofree; Trey Ideker
Journal:  Curr Opin Genet Dev       Date:  2013-11-14       Impact factor: 5.578

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.