Literature DB >> 30901550

Genomic Analysis in the Age of Human Genome Sequencing.

Tuuli Lappalainen1, Alexandra J Scott2, Margot Brandt3, Ira M Hall4.   

Abstract

Affordable genome sequencing technologies promise to revolutionize the field of human genetics by enabling comprehensive studies that interrogate all classes of genome variation, genome-wide, across the entire allele frequency spectrum. Ongoing projects worldwide are sequencing many thousands-and soon millions-of human genomes as part of various gene mapping studies, biobanking efforts, and clinical programs. However, while genome sequencing data production has become routine, genome analysis and interpretation remain challenging endeavors with many limitations and caveats. Here, we review the current state of technologies for genetic variant discovery, genotyping, and functional interpretation and discuss the prospects for future advances. We focus on germline variants discovered by whole-genome sequencing, genome-wide functional genomic approaches for predicting and measuring variant functional effects, and implications for studies of common and rare human disease.
Copyright © 2019 Elsevier Inc. All rights reserved.

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Year:  2019        PMID: 30901550      PMCID: PMC6532068          DOI: 10.1016/j.cell.2019.02.032

Source DB:  PubMed          Journal:  Cell        ISSN: 0092-8674            Impact factor:   41.582


  92 in total

1.  Integrative approaches for large-scale transcriptome-wide association studies.

Authors:  Alexander Gusev; Arthur Ko; Huwenbo Shi; Gaurav Bhatia; Wonil Chung; Brenda W J H Penninx; Rick Jansen; Eco J C de Geus; Dorret I Boomsma; Fred A Wright; Patrick F Sullivan; Elina Nikkola; Marcus Alvarez; Mete Civelek; Aldons J Lusis; Terho Lehtimäki; Emma Raitoharju; Mika Kähönen; Ilkka Seppälä; Olli T Raitakari; Johanna Kuusisto; Markku Laakso; Alkes L Price; Päivi Pajukanta; Bogdan Pasaniuc
Journal:  Nat Genet       Date:  2016-02-08       Impact factor: 38.330

2.  Maximum entropy modeling of short sequence motifs with applications to RNA splicing signals.

Authors:  Gene Yeo; Christopher B Burge
Journal:  J Comput Biol       Date:  2004       Impact factor: 1.479

Review 3.  Genome structural variation discovery and genotyping.

Authors:  Can Alkan; Bradley P Coe; Evan E Eichler
Journal:  Nat Rev Genet       Date:  2011-03-01       Impact factor: 53.242

Review 4.  10 Years of GWAS Discovery: Biology, Function, and Translation.

Authors:  Peter M Visscher; Naomi R Wray; Qian Zhang; Pamela Sklar; Mark I McCarthy; Matthew A Brown; Jian Yang
Journal:  Am J Hum Genet       Date:  2017-07-06       Impact factor: 11.025

5.  Large multiallelic copy number variations in humans.

Authors:  Robert E Handsaker; Vanessa Van Doren; Jennifer R Berman; Giulio Genovese; Seva Kashin; Linda M Boettger; Steven A McCarroll
Journal:  Nat Genet       Date:  2015-01-26       Impact factor: 38.330

6.  Cypiripi: exact genotyping of CYP2D6 using high-throughput sequencing data.

Authors:  Ibrahim Numanagić; Salem Malikić; Victoria M Pratt; Todd C Skaar; David A Flockhart; S Cenk Sahinalp
Journal:  Bioinformatics       Date:  2015-06-15       Impact factor: 6.937

7.  The landscape of human STR variation.

Authors:  Thomas Willems; Melissa Gymrek; Gareth Highnam; David Mittelman; Yaniv Erlich
Journal:  Genome Res       Date:  2014-08-18       Impact factor: 9.043

8.  Pathogenic variants that alter protein code often disrupt splicing.

Authors:  Rachel Soemedi; Kamil J Cygan; Christy L Rhine; Jing Wang; Charlston Bulacan; John Yang; Pinar Bayrak-Toydemir; Jamie McDonald; William G Fairbrother
Journal:  Nat Genet       Date:  2017-04-17       Impact factor: 38.330

9.  DELLY: structural variant discovery by integrated paired-end and split-read analysis.

Authors:  Tobias Rausch; Thomas Zichner; Andreas Schlattl; Adrian M Stütz; Vladimir Benes; Jan O Korbel
Journal:  Bioinformatics       Date:  2012-09-15       Impact factor: 6.937

10.  Bayesian test for colocalisation between pairs of genetic association studies using summary statistics.

Authors:  Claudia Giambartolomei; Damjan Vukcevic; Eric E Schadt; Lude Franke; Aroon D Hingorani; Chris Wallace; Vincent Plagnol
Journal:  PLoS Genet       Date:  2014-05-15       Impact factor: 5.917

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  65 in total

Review 1.  Detecting Causal Variants in Mendelian Disorders Using Whole-Genome Sequencing.

Authors:  Abdul Rezzak Hamzeh; T Daniel Andrews; Matt A Field
Journal:  Methods Mol Biol       Date:  2021

Review 2.  Genetics of Childhood-onset Schizophrenia 2019 Update.

Authors:  Jennifer K Forsyth; Robert F Asarnow
Journal:  Child Adolesc Psychiatr Clin N Am       Date:  2019-10-17

Review 3.  Clinical utility of genomic sequencing.

Authors:  Matthew B Neu; Kevin M Bowling; Gregory M Cooper
Journal:  Curr Opin Pediatr       Date:  2019-12       Impact factor: 2.856

4.  VIPdb, a genetic Variant Impact Predictor Database.

Authors:  Zhiqiang Hu; Changhua Yu; Mabel Furutsuki; Gaia Andreoletti; Melissa Ly; Roger Hoskins; Aashish N Adhikari; Steven E Brenner
Journal:  Hum Mutat       Date:  2019-08-17       Impact factor: 4.878

5.  A mutation map for human glycoside hydrolase genes.

Authors:  Lars Hansen; Diab M Husein; Birthe Gericke; Torben Hansen; Oluf Pedersen; Mitali A Tambe; Hudson H Freeze; Hassan Y Naim; Bernard Henrissat; Hans H Wandall; Henrik Clausen; Eric P Bennett
Journal:  Glycobiology       Date:  2020-07-16       Impact factor: 4.313

Review 6.  Functional genomics links genetic origins to pathophysiology in neurodegenerative and neuropsychiatric disease.

Authors:  Brie Wamsley; Daniel H Geschwind
Journal:  Curr Opin Genet Dev       Date:  2020-07-04       Impact factor: 5.578

Review 7.  Structural variation in the sequencing era.

Authors:  Steve S Ho; Alexander E Urban; Ryan E Mills
Journal:  Nat Rev Genet       Date:  2019-11-15       Impact factor: 53.242

Review 8.  'There and Back Again'-Forward Genetics and Reverse Phenotyping in Pulmonary Arterial Hypertension.

Authors:  Emilia M Swietlik; Matina Prapa; Jennifer M Martin; Divya Pandya; Kathryn Auckland; Nicholas W Morrell; Stefan Gräf
Journal:  Genes (Basel)       Date:  2020-11-26       Impact factor: 4.096

Review 9.  A Systematic Literature Review of Whole Exome and Genome Sequencing Population Studies of Genetic Susceptibility to Cancer.

Authors:  Alisa M Goldstein; Elizabeth M Gillanders; Melissa Rotunno; Rolando Barajas; Mindy Clyne; Elise Hoover; Naoko I Simonds; Tram Kim Lam; Leah E Mechanic
Journal:  Cancer Epidemiol Biomarkers Prev       Date:  2020-05-28       Impact factor: 4.254

10.  Allelic Heterogeneity at the CRP Locus Identified by Whole-Genome Sequencing in Multi-ancestry Cohorts.

Authors:  Laura M Raffield; Apoorva K Iyengar; Biqi Wang; Sheila M Gaynor; Cassandra N Spracklen; Xue Zhong; Madeline H Kowalski; Shabnam Salimi; Linda M Polfus; Emelia J Benjamin; Joshua C Bis; Russell Bowler; Brian E Cade; Won Jung Choi; Alejandro P Comellas; Adolfo Correa; Pedro Cruz; Harsha Doddapaneni; Peter Durda; Stephanie M Gogarten; Deepti Jain; Ryan W Kim; Brian G Kral; Leslie A Lange; Martin G Larson; Cecelia Laurie; Jiwon Lee; Seonwook Lee; Joshua P Lewis; Ginger A Metcalf; Braxton D Mitchell; Zeineen Momin; Donna M Muzny; Nathan Pankratz; Cheol Joo Park; Stephen S Rich; Jerome I Rotter; Kathleen Ryan; Daekwan Seo; Russell P Tracy; Karine A Viaud-Martinez; Lisa R Yanek; Lue Ping Zhao; Xihong Lin; Bingshan Li; Yun Li; Josée Dupuis; Alexander P Reiner; Karen L Mohlke; Paul L Auer
Journal:  Am J Hum Genet       Date:  2019-12-26       Impact factor: 11.025

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