Inventaire - 友達とコミュニティはあなたのベストな図書館です - Inventaire

Extremely low-coverage whole genome sequencing in South Asians captures population genomics information

著者

Erika Gedvilaite

Naveen Ramesh

Jinchuan Xing

Lynn Jorde

Donna Muzny

Shuoguo Wang

Scott E Watkins

この作品が含まれる作品: BMC Genomics

出版日: 2017-05-22

言語: 英語

main subject: 全ゲノム配列決定, ゲノミクス

Cites articles 51

Date

タイトル

著者

2016-07-04

Genome-wide association of multiple complex traits in outbred mice by ultra-low-coverage sequencing

Paul K Potter, Na Cai, Elisabeth M Lodder, Jennifer S Gregory, Amarjit Bhomra, Richard M. Aspden, Nick P Talbot, Paul Franken, Richard Mott
2016-07-04

Rapid genotype imputation from sequence without reference panels

Richard Mott, Jonathan Flint, Simon Myers
2016-05-01

Coming of age: ten years of next-generation sequencing technologies

ジョン・マクファーソン
2016-01-25

Genomic reconstruction of the history of extant populations of India reveals five distinct ancestral components and a complex structure

Partha P Majumder
2016-01-07

Genotype Imputation with Millions of Reference Samples

Sharon Browning
2015-10-01

A global reference for human genetic variation

Adam Auton, Shane McCarthy, リチャード・ダービン, 1000人ゲノムプロジェクト
2015-07-30

Sparse whole-genome sequencing identifies two loci for major depressive disorder
2015-07-01

Vestiges of an Ancient Border in the Contemporary Genetic Diversity of North-Eastern Europe

Antti Sajantila, Mikko Putkonen, Tarja Sundell
2014-11-25

ANGSD: Analysis of Next Generation Sequencing Data

Anders Albrechtsen, Thorfinn Korneliussen, Rasmus Nielsen
2014-05-15

Insights into the genetic structure and diversity of 38 South Asian Indians from deep whole-genome sequencing

Jason Kuan Han Lai, Peng Chen, Jia Nee Foo, Richie Soong, Chiea Chuen Khor
2014-03-16

Ancestry estimation and control of population stratification for sequence-based association studies

Anand Swaroop, Dwight Stambolian, Emily Chew, Elaine Mardis, Xihong Lin
2014-01-29

Launching genomics into the cloud: deployment of Mercury, a next generation sequence analysis pipeline

Eric Boerwinkle, Donna Muzny
2013-09-11

Estimating individual admixture proportions from next generation sequencing data

Thorfinn Korneliussen, Line Skotte, Anders Albrechtsen
2013-08-26

Quantifying population genetic differentiation from next-generation sequencing data

Rasmus Nielsen, Thorfinn Korneliussen, Filipe G. Vieira, Matteo Fumagalli, Anders Albrechtsen
2013-07-09

SNP ascertainment bias in population genetic analyses: why it is important, and how to correct it.

Joseph Lachance
2013-05-01

Genomic and epigenomic landscapes of adult de novo acute myeloid leukemia

Julie Gastier-Foster, Miruna Balasundaram, Yaron Butterfield, Gad Getz, Carrie Sougnez, Stacey Gabriel, Inanc Birol, Cyriac Kandoth, アンドルー・マンゴール, Steven Jones, Cancer Genome Atlas Research Network, Tanja M Davidsen, Stephen B. Baylin, Joshua F. McMichael, Lucinda Fulton, Kenna Mills Shaw, Readman Chiu
2013-01-07

An integrative variant analysis pipeline for accurate genotype/haplotype inference in population NGS data

Jin Yu
2012-11-01

An integrated map of genetic variation from 1,092 human genomes

Gilean McVean, Gonçalo Abecasis, リチャード・ダービン, Adam Auton, Robert E Handsaker, Vineet Bafna, Klaudia Walter, Andrew G. Clark, Andrea Angius, Matthew Hurles, Gabor T Marth
2012-05-20

Extremely low-coverage sequencing and imputation increases power for genome-wide association studies

Paul J. McLaren, Heng Li, Sarah E Bergen, Jennifer L. Moran, Patrik K E Magnusson, Bogdan Pasaniuc, Paul Lichtenstein, Christina M. Hultman, Mark Joseph Daly, Noah Zaitlen, Patrick F. Sullivan, Pamela Sklar, Nick Patterson, デイヴィッド・ライク, Nadin Rohland, Benjamin M. Neale, Alkes Price, Shaun M Purcell, Namrata Gupta, Paul I W de Bakker, Shamil R Sunyaev
2012-05-20

Exome sequencing generates high quality data in non-target regions

Wei Zheng, Qiuyin Cai, Xiao-Ou Shu
2012-01-20

Cost-effective, high-throughput DNA sequencing libraries for multiplexed target capture

デイヴィッド・ライク, Nadin Rohland
2011-08-01

The variant call format and VCFtools

リチャード・ダービン, Klaudia Walter, Andreas Dahl, Vineet Bafna
2011-04-01

Low-coverage sequencing: implications for design of complex trait association studies

Carlo Sidore, Gonçalo Abecasis, Michael Boehnke
2010

Genetic diversity in India and the inference of Eurasian population expansion

Lynn Jorde, Donna Muzny
2010-09-01

Integrating common and rare genetic variation in diverse human populations

Panos Deloukas, Sarah E. Hunt, Kyle Chang, Chris Barnes, Kati Kristiansson, Nicole Soranzo, Claudia Gonzaga-Jauregui, Verneri Anttila, William M McLaren, Clement Adebamowo, Julio Licinio, パルディス・サベティ, Stephen F Schaffner, Michael Inouye, レーナ・ペルトネン＝パロティエ, Mark Joseph Daly, Matthew Hurles, Vivian Ota Wang, Lora Lewis, Alicia Hawes, David A. Wheeler, Stephen Leslie
2010-09

The Genome Analysis Toolkit: A MapReduce framework for analyzing next-generation DNA sequencing data

David Altshuler, Kristian Cibulskis, Stacey Gabriel, Aaron McKenna, Mark Joseph Daly, Andrey Sivachenko, Eric Banks, Andrew Kernytsky, Mark DePristo
2010-04

A method and server for predicting damaging missense mutations

Peer Bork, Leonid Peshkin
2010-02-18

Limited distribution of a cardiomyopathy-associated variant in India

Jinchuan Xing, Lynn Jorde, Chad D. Huff, Tatum S Simonson, Scott E Watkins
2010-01-15

Fast and accurate long-read alignment with Burrows-Wheeler transform

Heng Li, リチャード・ダービン
2009-02

Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) Consortium: Design of prospective meta-analyses of genome-wide association studies from 5 cohorts

Vilmundur Gudnason, André Uitterlinden, Bruce M. Psaty, Eric Boerwinkle, Kathryn L. Lunetta, Jerome I Rotter, Tamara B. Harris, Aaron R. Folsom, Jacqueline C M Witteman
2009-09-24

Reconstructing Indian population history

デイヴィッド・ライク, Lalji Singh, Kumarasamy Thangaraj, Nick Patterson, Alkes Price
2009-09

Fast model-based estimation of ancestry in unrelated individuals

記事 - wd:Q33716821

Welcome to Inventaire

友達やコミュニティの図書館

もっと調べる

you are offline