Literature DB >> 16152676

Direct genomic selection.

Stavros Bashiardes1, Rose Veile, Cynthia Helms, Elaine R Mardis, Anne M Bowcock, Michael Lovett.   

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Year:  2005        PMID： 16152676     DOI： 10.1038/nmeth0105-63

Source DB:  PubMed          Journal:  Nat Methods        ISSN： 1548-7091            Impact factor:   28.547


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  39 in total

1.  Sequencing and analysis of Neanderthal genomic DNA.

Authors:  James P Noonan; Graham Coop; Sridhar Kudaravalli; Doug Smith; Johannes Krause; Joe Alessi; Feng Chen; Darren Platt; Svante Pääbo; Jonathan K Pritchard; Edward M Rubin
Journal:  Science       Date:  2006-11-17       Impact factor: 47.728

2.  High-throughput sequencing of microdissected chromosomal regions.

Authors:  Anja Weise; Bernd Timmermann; Manfred Grabherr; Martin Werber; Patricia Heyn; Nadezda Kosyakova; Thomas Liehr; Heidemarie Neitzel; Kateryna Konrat; Christiane Bommer; Carola Dietrich; Anna Rajab; Richard Reinhardt; Stefan Mundlos; Tom H Lindner; Katrin Hoffmann
Journal:  Eur J Hum Genet       Date:  2009-11-04       Impact factor: 4.246

3.  High-density nucleosome occupancy map of human chromosome 9p21-22 reveals chromatin organization of the type I interferon gene cluster.

Authors:  Jonathan E Freaney; Quanwei Zhang; Erbay Yigit; Rebecca Kim; Jonathan Widom; Ji-Ping Wang; Curt M Horvath
Journal:  J Interferon Cytokine Res       Date:  2014-03-27       Impact factor: 2.607

4.  Frequent mutation of BAP1 in metastasizing uveal melanomas.

Authors:  J William Harbour; Michael D Onken; Elisha D O Roberson; Shenghui Duan; Li Cao; Lori A Worley; M Laurin Council; Katie A Matatall; Cynthia Helms; Anne M Bowcock
Journal:  Science       Date:  2010-11-04       Impact factor: 47.728

Review 5.  Targeted deep resequencing of the human cancer genome using next-generation technologies.

Authors:  Samuel Myllykangas; Hanlee P Ji
Journal:  Biotechnol Genet Eng Rev       Date:  2010

Review 6.  Finding the fifth base: genome-wide sequencing of cytosine methylation.

Authors:  Ryan Lister; Joseph R Ecker
Journal:  Genome Res       Date:  2009-03-09       Impact factor: 9.043

7.  Combining microarray-based genomic selection (MGS) with the Illumina Genome Analyzer platform to sequence diploid target regions.

Authors:  David T Okou; Adam E Locke; Karyn M Steinberg; Katie Hagen; Prashanth Athri; Amol C Shetty; Viren Patel; Michael E Zwick
Journal:  Ann Hum Genet       Date:  2009-07-01       Impact factor: 1.670

8.  Detection of genomic variation by selection of a 9 mb DNA region and high throughput sequencing.

Authors:  Sergey I Nikolaev; Christian Iseli; Andrew J Sharp; Daniel Robyr; Jacques Rougemont; Corinne Gehrig; Laurent Farinelli; Stylianos E Antonarakis
Journal:  PLoS One       Date:  2009-08-17       Impact factor: 3.240

9.  Filter-based hybridization capture of subgenomes enables resequencing and copy-number detection.

Authors:  Daniel S Herman; G Kees Hovingh; Oleg Iartchouk; Heidi L Rehm; Raju Kucherlapati; J G Seidman; Christine E Seidman
Journal:  Nat Methods       Date:  2009-06-21       Impact factor: 28.547

10.  Improving the efficiency of genomic loci capture using oligonucleotide arrays for high throughput resequencing.

Authors:  Hane Lee; Brian D O'Connor; Barry Merriman; Vincent A Funari; Nils Homer; Zugen Chen; Daniel H Cohn; Stanley F Nelson
Journal:  BMC Genomics       Date:  2009-12-31       Impact factor: 3.969
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