Literature DB >> 21379402

Microarray oligonucleotide probe designer (MOPeD): A web service.

Viren C Patel1, Kajari Mondal, Amol Carl Shetty, Vanessa L Horner, Jirair K Bedoyan, Donna Martin, Tamara Caspary, David J Cutler, Michael E Zwick.   

Abstract

Methods of genomic selection that combine high-density oligonucleotide microarrays with next-generation DNA sequencing allow investigators to characterize genomic variation in selected portions of complex eukaryotic genomes. Yet choosing which specific oligonucleotides to be use can pose a major technical challenge. To address this issue, we have developed a software package called MOPeD (Microarray Oligonucleotide Probe Designer), which automates the process of designing genomic selection microarrays. This web-based software allows individual investigators to design custom genomic selection microarrays optimized for synthesis with Roche NimbleGen's maskless photolithography. Design parameters include uniqueness of the probe sequences, melting temperature, hairpin formation, and the presence of single nucleotide polymorphisms. We generated probe databases for the human, mouse, and rhesus macaque genomes and conducted experimental validation of MOPeD-designed microarrays in human samples by sequencing the human X chromosome exome, where relevant sequence metrics indicated superior performance relative to a microarray designed by the Roche NimbleGen proprietary algorithm. We also performed validation in the mouse to identify known mutations contained within a 487-kb region from mouse chromosome 16, the mouse chromosome 16 exome (1.7 Mb), and the mouse chromosome 12 exome (3.3 Mb). Our results suggest that the open source MOPeD software package and website (http://moped.genetics.emory.edu/) will make a valuable resource for investigators in their sequence-based studies of complex eukaryotic genomes.

Entities:  

Year:  2010        PMID: 21379402      PMCID: PMC3048354          DOI: 10.2147/OAB.S13741

Source DB:  PubMed          Journal:  Open Access Bioinformatics        ISSN: 1179-2701


  25 in total

1.  High-throughput variation detection and genotyping using microarrays.

Authors:  D J Cutler; M E Zwick; M M Carrasquillo; C T Yohn; K P Tobin; C Kashuk; D J Mathews; N A Shah; E E Eichler; J A Warrington; A Chakravarti
Journal:  Genome Res       Date:  2001-11       Impact factor: 9.043

2.  Theoretical aspects of genomic variation screening using DNA microarrays.

Authors:  Arnold Vainrub; B Montgomery Pettitt
Journal:  Biopolymers       Date:  2004-04-05       Impact factor: 2.505

Review 3.  Target-enrichment strategies for next-generation sequencing.

Authors:  Lira Mamanova; Alison J Coffey; Carol E Scott; Iwanka Kozarewa; Emily H Turner; Akash Kumar; Eleanor Howard; Jay Shendure; Daniel J Turner
Journal:  Nat Methods       Date:  2010-02       Impact factor: 28.547

4.  Direct genomic selection.

Authors:  Stavros Bashiardes; Rose Veile; Cynthia Helms; Elaine R Mardis; Anne M Bowcock; Michael Lovett
Journal:  Nat Methods       Date:  2005-01       Impact factor: 28.547

5.  Direct selection of human genomic loci by microarray hybridization.

Authors:  Thomas J Albert; Michael N Molla; Donna M Muzny; Lynne Nazareth; David Wheeler; Xingzhi Song; Todd A Richmond; Chris M Middle; Matthew J Rodesch; Charles J Packard; George M Weinstock; Richard A Gibbs
Journal:  Nat Methods       Date:  2007-10-14       Impact factor: 28.547

6.  Empirical evaluation of oligonucleotide probe selection for DNA microarrays.

Authors:  Jennifer G Mulle; Viren C Patel; Stephen T Warren; Madhuri R Hegde; David J Cutler; Michael E Zwick
Journal:  PLoS One       Date:  2010-03-29       Impact factor: 3.240

7.  The graded response to Sonic Hedgehog depends on cilia architecture.

Authors:  Tamara Caspary; Christine E Larkins; Kathryn V Anderson
Journal:  Dev Cell       Date:  2007-05       Impact factor: 12.270

8.  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

9.  Multiplex amplification of large sets of human exons.

Authors:  Gregory J Porreca; Kun Zhang; Jin Billy Li; Bin Xie; Derek Austin; Sara L Vassallo; Emily M LeProust; Bill J Peck; Christopher J Emig; Fredrik Dahl; Yuan Gao; George M Church; Jay Shendure
Journal:  Nat Methods       Date:  2007-10-14       Impact factor: 28.547

10.  Solution hybrid selection with ultra-long oligonucleotides for massively parallel targeted sequencing.

Authors:  Andreas Gnirke; Alexandre Melnikov; Jared Maguire; Peter Rogov; Emily M LeProust; William Brockman; Timothy Fennell; Georgia Giannoukos; Sheila Fisher; Carsten Russ; Stacey Gabriel; David B Jaffe; Eric S Lander; Chad Nusbaum
Journal:  Nat Biotechnol       Date:  2009-02-01       Impact factor: 54.908

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  4 in total

1.  Targeted sequencing of the human X chromosome exome.

Authors:  Kajari Mondal; Amol Carl Shetty; Viren Patel; David J Cutler; Michael E Zwick
Journal:  Genomics       Date:  2011-04-16       Impact factor: 5.736

2.  Multiplex Chromosomal Exome Sequencing Accelerates Identification of ENU-Induced Mutations in the Mouse.

Authors:  Miao Sun; Kajari Mondal; Viren Patel; Vanessa L Horner; Alyssa B Long; David J Cutler; Tamara Caspary; Michael E Zwick
Journal:  G3 (Bethesda)       Date:  2012-01-01       Impact factor: 3.154

Review 3.  Targeted enrichment of genomic DNA regions for next-generation sequencing.

Authors:  Florian Mertes; Abdou Elsharawy; Sascha Sauer; Joop M L M van Helvoort; P J van der Zaag; Andre Franke; Mats Nilsson; Hans Lehrach; Anthony J Brookes
Journal:  Brief Funct Genomics       Date:  2011-11-26       Impact factor: 4.241

4.  Disruption of RAB40AL function leads to Martin--Probst syndrome, a rare X-linked multisystem neurodevelopmental human disorder.

Authors:  Jirair Krikor Bedoyan; Valerie M Schaibley; Weiping Peng; Yongsheng Bai; Kajari Mondal; Amol C Shetty; Mark Durham; Joseph A Micucci; Arti Dhiraaj; Jennifer M Skidmore; Julie B Kaplan; Cindy Skinner; Charles E Schwartz; Anthony Antonellis; Michael E Zwick; James D Cavalcoli; Jun Z Li; Donna M Martin
Journal:  J Med Genet       Date:  2012-05       Impact factor: 6.318

  4 in total

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