Literature DB >> 19630561

Methods for genomic partitioning.

Emily H Turner1, Sarah B Ng, Deborah A Nickerson, Jay Shendure.   

Abstract

The emergence of massively parallel DNA sequencing platforms has made resequencing an affordable approach to study genetic variation. However, the cost of whole genome resequencing remains too high to apply to large numbers of human samples. Genomic partitioning methods allow enrichment for regions of interest at a scale that is matched to the throughput of the new sequencing platforms. We review general categories of methods for genomic partitioning including multiplex PCR, capture-by-circularization, and capture-by-hybridization. Parameters that are relevant to the performance of any given method include multiplexity, specificity, uniformity, input requirements, scalability, and cost. The successful development of genomic partitioning strategies will be key to taking full advantage of massively parallel sequencing, at least until resequencing of complete mammalian genomes becomes widely affordable.

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Year:  2009        PMID: 19630561     DOI: 10.1146/annurev-genom-082908-150112

Source DB:  PubMed          Journal:  Annu Rev Genomics Hum Genet        ISSN: 1527-8204            Impact factor:   8.929


  45 in total

1.  Systematic comparison of three genomic enrichment methods for massively parallel DNA sequencing.

Authors:  Jamie K Teer; Lori L Bonnycastle; Peter S Chines; Nancy F Hansen; Natsuyo Aoyama; Amy J Swift; Hatice Ozel Abaan; Thomas J Albert; Elliott H Margulies; Eric D Green; Francis S Collins; James C Mullikin; Leslie G Biesecker
Journal:  Genome Res       Date:  2010-09-01       Impact factor: 9.043

Review 2.  Massively parallel sequencing: the new frontier of hematologic genomics.

Authors:  Jill M Johnsen; Deborah A Nickerson; Alex P Reiner
Journal:  Blood       Date:  2013-09-10       Impact factor: 22.113

3.  PCR-activated cell sorting as a general, cultivation-free method for high-throughput identification and enrichment of virus hosts.

Authors:  Shaun W Lim; Shea T Lance; Kenneth M Stedman; Adam R Abate
Journal:  J Virol Methods       Date:  2016-12-29       Impact factor: 2.014

4.  Accurate detection and genotyping of SNPs utilizing population sequencing data.

Authors:  Vikas Bansal; Olivier Harismendy; Ryan Tewhey; Sarah S Murray; Nicholas J Schork; Eric J Topol; Kelly A Frazer
Journal:  Genome Res       Date:  2010-02-11       Impact factor: 9.043

Review 5.  Next-generation hybridization and introgression.

Authors:  A D Twyford; R A Ennos
Journal:  Heredity (Edinb)       Date:  2011-09-07       Impact factor: 3.821

Review 6.  Exome sequencing as a tool for Mendelian disease gene discovery.

Authors:  Michael J Bamshad; Sarah B Ng; Abigail W Bigham; Holly K Tabor; Mary J Emond; Deborah A Nickerson; Jay Shendure
Journal:  Nat Rev Genet       Date:  2011-09-27       Impact factor: 53.242

7.  Identification of gene mutations in autosomal dominant polycystic kidney disease through targeted resequencing.

Authors:  Sandro Rossetti; Katharina Hopp; Robert A Sikkink; Jamie L Sundsbak; Yean Kit Lee; Vickie Kubly; Bruce W Eckloff; Christopher J Ward; Christopher G Winearls; Vicente E Torres; Peter C Harris
Journal:  J Am Soc Nephrol       Date:  2012-03-01       Impact factor: 10.121

8.  Targeted sequencing for gene discovery and quantification using RNA CaptureSeq.

Authors:  Tim R Mercer; Michael B Clark; Joanna Crawford; Marion E Brunck; Daniel J Gerhardt; Ryan J Taft; Lars K Nielsen; Marcel E Dinger; John S Mattick
Journal:  Nat Protoc       Date:  2014-04-03       Impact factor: 13.491

9.  Targeted enrichment of specific regions in the human genome by array hybridization.

Authors:  Catherine Igartua; Emily H Turner; Sarah B Ng; Emily Hodges; Gregory J Hannon; Arindam Bhattacharjee; Mark J Rieder; Deborah A Nickerson; Jay Shendure
Journal:  Curr Protoc Hum Genet       Date:  2010-07

10.  Next generation sequence analysis for mitochondrial disorders.

Authors:  Valeria Vasta; Sarah B Ng; Emily H Turner; Jay Shendure; Si Houn Hahn
Journal:  Genome Med       Date:  2009-10-23       Impact factor: 11.117

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