Literature DB >> 20938837

Mutation surveyor: software for DNA sequence analysis.

Jayne A L Minton1, Sarah E Flanagan, Sian Ellard.   

Abstract

Advances in high-throughput sequencing techniques had presented a significant challenge to the processing capabilities of genetic laboratories. However, recent developments in the field of semi-automated mutation detection have revolutionised the task of mutation detection.This chapter provides user information for one commercially available program, Mutation Surveyor. The software is manufactured by SoftGenetics (Pennsylvania, USA) and provides an accurate and efficient program for detecting sequence variants. The chapter focuses on the methodology of setting up GenBank files as reference files and provides information on analysis parameters and data processing.

Mesh:

Year:  2011        PMID: 20938837     DOI: 10.1007/978-1-60761-947-5_10

Source DB:  PubMed          Journal:  Methods Mol Biol        ISSN: 1064-3745


  18 in total

1.  Genome-wide SNP genotyping identifies the Stereocilin (STRC) gene as a major contributor to pediatric bilateral sensorineural hearing impairment.

Authors:  Lauren J Francey; Laura K Conlin; Hanna E Kadesch; Dinah Clark; Donna Berrodin; Yi Sun; Joe Glessner; Hakon Hakonarson; Chaim Jalas; Chaim Landau; Nancy B Spinner; Margaret Kenna; Michal Sagi; Heidi L Rehm; Ian D Krantz
Journal:  Am J Med Genet A       Date:  2011-12-06       Impact factor: 2.802

2.  Crossovers are associated with mutation and biased gene conversion at recombination hotspots.

Authors:  Barbara Arbeithuber; Andrea J Betancourt; Thomas Ebner; Irene Tiemann-Boege
Journal:  Proc Natl Acad Sci U S A       Date:  2015-02-02       Impact factor: 11.205

3.  Identification and Evaluation of Single-Nucleotide Polymorphisms in Allotetraploid Peanut (Arachis hypogaea L.) Based on Amplicon Sequencing Combined with High Resolution Melting (HRM) Analysis.

Authors:  Yanbin Hong; Manish K Pandey; Ying Liu; Xiaoping Chen; Hong Liu; Rajeev K Varshney; Xuanqiang Liang; Shangzhi Huang
Journal:  Front Plant Sci       Date:  2015-12-02       Impact factor: 5.753

4.  Noninvasive detection of tumor-associated mutations from circulating cell-free DNA in hepatocellular carcinoma patients by targeted deep sequencing.

Authors:  Wenjun Liao; Huayu Yang; Haifeng Xu; Yanan Wang; Penglei Ge; Jinjun Ren; Wei Xu; Xin Lu; Xinting Sang; Shouxian Zhong; Hongbing Zhang; Yilei Mao
Journal:  Oncotarget       Date:  2016-06-28

5.  Artifactual mutations resulting from DNA lesions limit detection levels in ultrasensitive sequencing applications.

Authors:  Barbara Arbeithuber; Kateryna D Makova; Irene Tiemann-Boege
Journal:  DNA Res       Date:  2016-07-31       Impact factor: 4.458

6.  An Ultraconserved Element (UCE) controls homeostatic splicing of ARGLU1 mRNA.

Authors:  Stephan P Pirnie; Ahmad Osman; Yinzhou Zhu; Gordon G Carmichael
Journal:  Nucleic Acids Res       Date:  2017-04-07       Impact factor: 16.971

7.  Integrated genomics approach to identify biologically relevant alterations in fewer samples.

Authors:  Pratik Chandrani; Pawan Upadhyay; Prajish Iyer; Mayur Tanna; Madhur Shetty; Gorantala Venkata Raghuram; Ninad Oak; Ankita Singh; Rohan Chaubal; Manoj Ramteke; Sudeep Gupta; Amit Dutt
Journal:  BMC Genomics       Date:  2015-11-14       Impact factor: 3.969

8.  Somatic Mutations and Genetic Variants of NOTCH1 in Head and Neck Squamous Cell Carcinoma Occurrence and Development.

Authors:  Yu-Fan Liu; Shang-Lun Chiang; Chien-Yu Lin; Jan-Gowth Chang; Chia-Min Chung; Albert Min-Shan Ko; You-Zhe Lin; Chien-Hung Lee; Ka-Wo Lee; Mu-Kuan Chen; Chun-Hung Hua; Ming-Hsui Tsai; Yuan-Chien Chen; Ying-Chin Ko
Journal:  Sci Rep       Date:  2016-04-01       Impact factor: 4.379

9.  CRE: a cost effective and rapid approach for PCR-mediated concatenation of KRAS and EGFR exons: Rapid way to detect EGFR and KRAS mutations.

Authors:  Manoj P Ramteke; Kuldeep J Patel; Mukul Godbole; Maulik Vyas; Kunal Karve; Anuradha Choughule; Kumar Prabhash; Amit Dutt
Journal:  F1000Res       Date:  2015-06-23

10.  MYOD1 (L122R) mutations are associated with spindle cell and sclerosing rhabdomyosarcomas with aggressive clinical outcomes.

Authors:  Bharat Rekhi; Pawan Upadhyay; Manoj P Ramteke; Amit Dutt
Journal:  Mod Pathol       Date:  2016-08-26       Impact factor: 7.842

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