Literature DB >> 20399638

Human allelic variation: perspective from protein function, structure, and evolution.

Daniel M Jordan1, Vasily E Ramensky, Shamil R Sunyaev.   

Abstract

It is widely anticipated that the coming year will be marked by the complete characterization of DNA sequence of protein-coding regions of thousands of human individuals. A number of existing computational methods use comparative protein sequence analysis and analysis of protein structure to predict the functional effect of coding human alleles. Functional and structural analysis of coding allelic variants can inform various aspects of research on human genetic variation. In population and evolutionary genetics it helps estimate the strength of purifying selection against deleterious missense mutations and study the imprint of demographic history on deleterious genetic variation. In medical genetics it may assist in the interpretation of uncharacterized mutations in genes involved in monogenic and oligogenic diseases. It has a potential to facilitate medical sequencing studies searching for genes underlying Mendelian diseases or harboring rare alleles involved in complex traits. Copyright 2010 Elsevier Ltd. All rights reserved.

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Year:  2010        PMID: 20399638      PMCID: PMC2921592          DOI: 10.1016/j.sbi.2010.03.006

Source DB:  PubMed          Journal:  Curr Opin Struct Biol        ISSN: 0959-440X            Impact factor:   6.809


  76 in total

1.  LS-SNP: large-scale annotation of coding non-synonymous SNPs based on multiple information sources.

Authors:  Rachel Karchin; Mark Diekhans; Libusha Kelly; Daryl J Thomas; Ursula Pieper; Narayanan Eswar; David Haussler; Andrej Sali
Journal:  Bioinformatics       Date:  2005-04-12       Impact factor: 6.937

2.  Simultaneous inference of selection and population growth from patterns of variation in the human genome.

Authors:  Scott H Williamson; Ryan Hernandez; Adi Fledel-Alon; Lan Zhu; Rasmus Nielsen; Carlos D Bustamante
Journal:  Proc Natl Acad Sci U S A       Date:  2005-05-19       Impact factor: 11.205

3.  Compensated deleterious mutations in insect genomes.

Authors:  Rob J Kulathinal; Brian R Bettencourt; Daniel L Hartl
Journal:  Science       Date:  2004-10-21       Impact factor: 47.728

4.  A method and server for predicting damaging missense mutations.

Authors:  Ivan A Adzhubei; Steffen Schmidt; Leonid Peshkin; Vasily E Ramensky; Anna Gerasimova; Peer Bork; Alexey S Kondrashov; Shamil R Sunyaev
Journal:  Nat Methods       Date:  2010-04       Impact factor: 28.547

5.  A survey of proteins encoded by non-synonymous single nucleotide polymorphisms reveals a significant fraction with altered stability and activity.

Authors:  Abdellah Allali-Hassani; Gregory A Wasney; Irene Chau; Bum Soo Hong; Guillermo Senisterra; Peter Loppnau; Zhen Shi; John Moult; Aled M Edwards; Cheryl H Arrowsmith; Hee Won Park; Matthieu Schapira; Masoud Vedadi
Journal:  Biochem J       Date:  2009-10-23       Impact factor: 3.857

6.  nsSNPAnalyzer: identifying disease-associated nonsynonymous single nucleotide polymorphisms.

Authors:  Lei Bao; Mi Zhou; Yan Cui
Journal:  Nucleic Acids Res       Date:  2005-07-01       Impact factor: 16.971

7.  I-Mutant2.0: predicting stability changes upon mutation from the protein sequence or structure.

Authors:  Emidio Capriotti; Piero Fariselli; Rita Casadio
Journal:  Nucleic Acids Res       Date:  2005-07-01       Impact factor: 16.971

8.  Structural and functional roles of coevolved sites in proteins.

Authors:  Saikat Chakrabarti; Anna R Panchenko
Journal:  PLoS One       Date:  2010-01-06       Impact factor: 3.240

9.  Bi-directional SIFT predicts a subset of activating mutations.

Authors:  William Lee; Yan Zhang; Kiran Mukhyala; Robert A Lazarus; Zemin Zhang
Journal:  PLoS One       Date:  2009-12-14       Impact factor: 3.240

10.  Exome sequencing identifies the cause of a mendelian disorder.

Authors:  Sarah B Ng; Kati J Buckingham; Choli Lee; Abigail W Bigham; Holly K Tabor; Karin M Dent; Chad D Huff; Paul T Shannon; Ethylin Wang Jabs; Deborah A Nickerson; Jay Shendure; Michael J Bamshad
Journal:  Nat Genet       Date:  2009-11-13       Impact factor: 38.330

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  35 in total

1.  Redesigning a library-based genetics class research project through instructional theory and authentic experience.

Authors:  Michele R Tennant; Mary Edwards; Michael M Miyamoto
Journal:  J Med Libr Assoc       Date:  2012-04

2.  Exome sequencing and the genetic basis of complex traits.

Authors:  Adam Kiezun; Kiran Garimella; Ron Do; Nathan O Stitziel; Benjamin M Neale; Paul J McLaren; Namrata Gupta; Pamela Sklar; Patrick F Sullivan; Jennifer L Moran; Christina M Hultman; Paul Lichtenstein; Patrik Magnusson; Thomas Lehner; Yin Yao Shugart; Alkes L Price; Paul I W de Bakker; Shaun M Purcell; Shamil R Sunyaev
Journal:  Nat Genet       Date:  2012-05-29       Impact factor: 38.330

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.  Development and validation of a computational method for assessment of missense variants in hypertrophic cardiomyopathy.

Authors:  Daniel M Jordan; Adam Kiezun; Samantha M Baxter; Vineeta Agarwala; Robert C Green; Michael F Murray; Trevor Pugh; Matthew S Lebo; Heidi L Rehm; Birgit H Funke; Shamil R Sunyaev
Journal:  Am J Hum Genet       Date:  2011-02-11       Impact factor: 11.025

Review 5.  Inferring causality and functional significance of human coding DNA variants.

Authors:  Shamil R Sunyaev
Journal:  Hum Mol Genet       Date:  2012-09-17       Impact factor: 6.150

6.  Prediction of missense mutation functionality depends on both the algorithm and sequence alignment employed.

Authors:  Stephanie Hicks; David A Wheeler; Sharon E Plon; Marek Kimmel
Journal:  Hum Mutat       Date:  2011-04-07       Impact factor: 4.878

7.  The Damaging Effect of Passenger Mutations on Cancer Progression.

Authors:  Christopher D McFarland; Julia A Yaglom; Jonathan W Wojtkowiak; Jacob G Scott; David L Morse; Michael Y Sherman; Leonid A Mirny
Journal:  Cancer Res       Date:  2017-05-23       Impact factor: 12.701

8.  Tug-of-war between driver and passenger mutations in cancer and other adaptive processes.

Authors:  Christopher D McFarland; Leonid A Mirny; Kirill S Korolev
Journal:  Proc Natl Acad Sci U S A       Date:  2014-10-02       Impact factor: 11.205

9.  Chip-based direct genotyping of coding variants in genome wide association studies: utility, issues and prospects.

Authors:  Caroline M Nievergelt; Nathan E Wineinger; Ondrej Libiger; Phillip Pham; Guangfa Zhang; Dewleen G Baker; Nicholas J Schork
Journal:  Gene       Date:  2014-02-09       Impact factor: 3.688

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

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