Literature DB >> 24867941

MIPgen: optimized modeling and design of molecular inversion probes for targeted resequencing.

Evan A Boyle1, Brian J O'Roak1, Beth K Martin1, Akash Kumar1, Jay Shendure1.   

Abstract

UNLABELLED: Molecular inversion probes (MIPs) enable cost-effective multiplex targeted gene resequencing in large cohorts. However, the design of individual MIPs is a critical parameter governing the performance of this technology with respect to capture uniformity and specificity. MIPgen is a user-friendly package that simplifies the process of designing custom MIP assays to arbitrary targets. New logistic and SVM-derived models enable in silico predictions of assay success, and assay redesign exhibits improved coverage uniformity relative to previous methods, which in turn improves the utility of MIPs for cost-effective targeted sequencing for candidate gene validation and for diagnostic sequencing in a clinical setting.
AVAILABILITY AND IMPLEMENTATION: MIPgen is implemented in C++. Source code and accompanying Python scripts are available at http://shendurelab.github.io/MIPGEN/.
© The Author 2014. Published by Oxford University Press. All rights reserved. For Permissions, please e-mail: journals.permissions@oup.com.

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Year:  2014        PMID: 24867941      PMCID: PMC4155255          DOI: 10.1093/bioinformatics/btu353

Source DB:  PubMed          Journal:  Bioinformatics        ISSN: 1367-4803            Impact factor:   6.937


  20 in total

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3.  A de novo paradigm for mental retardation.

Authors:  Lisenka E L M Vissers; Joep de Ligt; Christian Gilissen; Irene Janssen; Marloes Steehouwer; Petra de Vries; Bart van Lier; Peer Arts; Nienke Wieskamp; Marisol del Rosario; Bregje W M van Bon; Alexander Hoischen; Bert B A de Vries; Han G Brunner; Joris A Veltman
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4.  High-quality DNA sequence capture of 524 disease candidate genes.

Authors:  Peidong Shen; Wenyi Wang; Sujatha Krishnakumar; Curtis Palm; Aung-Kyaw Chi; Gregory M Enns; Ronald W Davis; Terence P Speed; Michael N Mindrinos; Curt Scharfe
Journal:  Proc Natl Acad Sci U S A       Date:  2011-04-05       Impact factor: 11.205

5.  Molecular inversion probes reveal patterns of 9p21 deletion and copy number aberrations in childhood leukemia.

Authors:  Joshua D Schiffman; Yuker Wang; Lisa A McPherson; Katrina Welch; Nancy Zhang; Ronald Davis; Norman J Lacayo; Gary V Dahl; Malek Faham; James M Ford; Hanlee P Ji
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6.  Targeted bisulfite sequencing reveals changes in DNA methylation associated with nuclear reprogramming.

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Journal:  Nat Biotechnol       Date:  2009-03-29       Impact factor: 54.908

7.  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

8.  Multiplex padlock targeted sequencing reveals human hypermutable CpG variations.

Authors:  Jin Billy Li; Yuan Gao; John Aach; Kun Zhang; Gregory V Kryukov; Bin Xie; Annika Ahlford; Jung-Ki Yoon; Abraham M Rosenbaum; Alexander Wait Zaranek; Emily LeProust; Shamil R Sunyaev; George M Church
Journal:  Genome Res       Date:  2009-06-12       Impact factor: 9.043

9.  Digital RNA allelotyping reveals tissue-specific and allele-specific gene expression in human.

Authors:  Kun Zhang; Jin Billy Li; Yuan Gao; Dieter Egli; Bin Xie; Jie Deng; Zhe Li; Je-Hyuk Lee; John Aach; Emily M Leproust; Kevin Eggan; George M Church
Journal:  Nat Methods       Date:  2009-07-20       Impact factor: 28.547

10.  Next-generation carrier screening.

Authors:  Mark A Umbarger; Caleb J Kennedy; Patrick Saunders; Benjamin Breton; Niru Chennagiri; John Emhoff; Valerie Greger; Stephanie Hallam; David Maganzini; Cynthia Micale; Marcia M Nizzari; Charles F Towne; George M Church; Gregory J Porreca
Journal:  Genet Med       Date:  2013-06-13       Impact factor: 8.822

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  65 in total

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Authors:  Davide Mei; Elena Parrini; Carla Marini; Renzo Guerrini
Journal:  Mol Diagn Ther       Date:  2017-08       Impact factor: 4.074

2.  Ultra-sensitive Sequencing Identifies High Prevalence of Clonal Hematopoiesis-Associated Mutations throughout Adult Life.

Authors:  Rocio Acuna-Hidalgo; Hilal Sengul; Marloes Steehouwer; Maartje van de Vorst; Sita H Vermeulen; Lambertus A L M Kiemeney; Joris A Veltman; Christian Gilissen; Alexander Hoischen
Journal:  Am J Hum Genet       Date:  2017-06-29       Impact factor: 11.025

3.  Genetic analysis of bleeding disorders.

Authors:  E Edison; B A Konkle; A C Goodeve
Journal:  Haemophilia       Date:  2016-07       Impact factor: 4.287

4.  RNA-based high-risk HPV genotyping and identification of high-risk HPV transcriptional activity in cervical tissues.

Authors:  Corina N A M van den Heuvel; Diede L Loopik; Renée M F Ebisch; Duaa Elmelik; Karolina M Andralojc; Martijn Huynen; Johan Bulten; Ruud L M Bekkers; Leon F A G Massuger; Willem J G Melchers; Albert G Siebers; William P J Leenders
Journal:  Mod Pathol       Date:  2019-09-19       Impact factor: 7.842

5.  Overrepresentation of genetic variation in the AnkyrinG interactome is related to a range of neurodevelopmental disorders.

Authors:  Ilse M van der Werf; Sandra Jansen; Petra F de Vries; Amber Gerstmans; Maartje van de Vorst; Anke Van Dijck; Bert B A de Vries; Christian Gilissen; Alexander Hoischen; Lisenka E L M Vissers; R Frank Kooy; Geert Vandeweyer
Journal:  Eur J Hum Genet       Date:  2020-07-10       Impact factor: 4.246

6.  De novo mutations in NALCN cause a syndrome characterized by congenital contractures of the limbs and face, hypotonia, and developmental delay.

Authors:  Jessica X Chong; Margaret J McMillin; Kathryn M Shively; Anita E Beck; Colby T Marvin; Jose R Armenteros; Kati J Buckingham; Naomi T Nkinsi; Evan A Boyle; Margaret N Berry; Maureen Bocian; Nicola Foulds; Maria Luisa Giovannucci Uzielli; Chad Haldeman-Englert; Raoul C M Hennekam; Paige Kaplan; Antonie D Kline; Catherine L Mercer; Malgorzata J M Nowaczyk; Jolien S Klein Wassink-Ruiter; Elizabeth W McPherson; Regina A Moreno; Angela E Scheuerle; Vandana Shashi; Cathy A Stevens; John C Carey; Arnaud Monteil; Philippe Lory; Holly K Tabor; Joshua D Smith; Jay Shendure; Deborah A Nickerson; Michael J Bamshad
Journal:  Am J Hum Genet       Date:  2015-02-12       Impact factor: 11.025

Review 7.  Enhancing the accuracy of next-generation sequencing for detecting rare and subclonal mutations.

Authors:  Jesse J Salk; Michael W Schmitt; Lawrence A Loeb
Journal:  Nat Rev Genet       Date:  2018-03-26       Impact factor: 53.242

8.  Novel approach to genetic analysis and results in 3000 hemophilia patients enrolled in the My Life, Our Future initiative.

Authors:  Jill M Johnsen; Shelley N Fletcher; Haley Huston; Sarah Roberge; Beth K Martin; Martin Kircher; Neil C Josephson; Jay Shendure; Sarah Ruuska; Marion A Koerper; Jaime Morales; Glenn F Pierce; Diane J Aschman; Barbara A Konkle
Journal:  Blood Adv       Date:  2017-05-18

9.  Exonic Mosaic Mutations Contribute Risk for Autism Spectrum Disorder.

Authors:  Deidre R Krupp; Rebecca A Barnard; Yannis Duffourd; Sara A Evans; Ryan M Mulqueen; Raphael Bernier; Jean-Baptiste Rivière; Eric Fombonne; Brian J O'Roak
Journal:  Am J Hum Genet       Date:  2017-08-31       Impact factor: 11.025

10.  Ultrasensitive Detection of Chimerism by Single-Molecule Molecular Inversion Probe Capture and High-Throughput Sequencing of Copy Number Deletion Polymorphisms.

Authors:  David Wu; Adam Waalkes; Kelsi Penewit; Stephen J Salipante
Journal:  Clin Chem       Date:  2018-03-16       Impact factor: 8.327

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