Literature DB >> 23620360

Shimmer: detection of genetic alterations in tumors using next-generation sequence data.

Nancy F Hansen1, Jared J Gartner, Lan Mei, Yardena Samuels, James C Mullikin.   

Abstract

MOTIVATION: Extensive DNA sequencing of tumor and matched normal samples using exome and whole-genome sequencing technologies has enabled the discovery of recurrent genetic alterations in cancer cells, but variability in stromal contamination and subclonal heterogeneity still present a severe challenge to available detection algorithms.
RESULTS: Here, we describe publicly available software, Shimmer, which accurately detects somatic single-nucleotide variants using statistical hypothesis testing with multiple testing correction. This program produces somatic single-nucleotide variant predictions with significantly higher sensitivity and accuracy than other available software when run on highly contaminated or heterogeneous samples, and it gives comparable sensitivity and accuracy when run on samples of high purity. AVAILABILITY: http://www.github.com/nhansen/Shimmer

Entities:  

Mesh:

Year:  2013        PMID: 23620360      PMCID: PMC3673219          DOI: 10.1093/bioinformatics/btt183

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


  28 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

2.  The mutation spectrum revealed by paired genome sequences from a lung cancer patient.

Authors:  William Lee; Zhaoshi Jiang; Jinfeng Liu; Peter M Haverty; Yinghui Guan; Jeremy Stinson; Peng Yue; Yan Zhang; Krishna P Pant; Deepali Bhatt; Connie Ha; Stephanie Johnson; Michael I Kennemer; Sankar Mohan; Igor Nazarenko; Colin Watanabe; Andrew B Sparks; David S Shames; Robert Gentleman; Frederic J de Sauvage; Howard Stern; Ajay Pandita; Dennis G Ballinger; Radoje Drmanac; Zora Modrusan; Somasekar Seshagiri; Zemin Zhang
Journal:  Nature       Date:  2010-05-27       Impact factor: 49.962

3.  Exome sequencing identifies GRIN2A as frequently mutated in melanoma.

Authors:  Xiaomu Wei; Vijay Walia; Jimmy C Lin; Jamie K Teer; Todd D Prickett; Jared Gartner; Sean Davis; Katherine Stemke-Hale; Michael A Davies; Jeffrey E Gershenwald; William Robinson; Steven Robinson; Steven A Rosenberg; Yardena Samuels
Journal:  Nat Genet       Date:  2011-04-15       Impact factor: 38.330

4.  A statistical framework for SNP calling, mutation discovery, association mapping and population genetical parameter estimation from sequencing data.

Authors:  Heng Li
Journal:  Bioinformatics       Date:  2011-09-08       Impact factor: 6.937

5.  Frequent mutations of chromatin remodeling genes in transitional cell carcinoma of the bladder.

Authors:  Yaoting Gui; Guangwu Guo; Yi Huang; Xueda Hu; Aifa Tang; Shengjie Gao; Renhua Wu; Chao Chen; Xianxin Li; Liang Zhou; Minghui He; Zesong Li; Xiaojuan Sun; Wenlong Jia; Jinnong Chen; Shangming Yang; Fangjian Zhou; Xiaokun Zhao; Shengqing Wan; Rui Ye; Chaozhao Liang; Zhisheng Liu; Peide Huang; Chunxiao Liu; Hui Jiang; Yong Wang; Hancheng Zheng; Liang Sun; Xingwang Liu; Zhimao Jiang; Dafei Feng; Jing Chen; Song Wu; Jing Zou; Zhongfu Zhang; Ruilin Yang; Jun Zhao; Congjie Xu; Weihua Yin; Zhichen Guan; Jiongxian Ye; Hong Zhang; Jingxiang Li; Karsten Kristiansen; Michael L Nickerson; Dan Theodorescu; Yingrui Li; Xiuqing Zhang; Songgang Li; Jian Wang; Huanming Yang; Jun Wang; Zhiming Cai
Journal:  Nat Genet       Date:  2011-08-07       Impact factor: 38.330

6.  A comprehensive catalogue of somatic mutations from a human cancer genome.

Authors:  Erin D Pleasance; R Keira Cheetham; Philip J Stephens; David J McBride; Sean J Humphray; Chris D Greenman; Ignacio Varela; Meng-Lay Lin; Gonzalo R Ordóñez; Graham R Bignell; Kai Ye; Julie Alipaz; Markus J Bauer; David Beare; Adam Butler; Richard J Carter; Lina Chen; Anthony J Cox; Sarah Edkins; Paula I Kokko-Gonzales; Niall A Gormley; Russell J Grocock; Christian D Haudenschild; Matthew M Hims; Terena James; Mingming Jia; Zoya Kingsbury; Catherine Leroy; John Marshall; Andrew Menzies; Laura J Mudie; Zemin Ning; Tom Royce; Ole B Schulz-Trieglaff; Anastassia Spiridou; Lucy A Stebbings; Lukasz Szajkowski; Jon Teague; David Williamson; Lynda Chin; Mark T Ross; Peter J Campbell; David R Bentley; P Andrew Futreal; Michael R Stratton
Journal:  Nature       Date:  2009-12-16       Impact factor: 49.962

7.  ANNOVAR: functional annotation of genetic variants from high-throughput sequencing data.

Authors:  Kai Wang; Mingyao Li; Hakon Hakonarson
Journal:  Nucleic Acids Res       Date:  2010-07-03       Impact factor: 16.971

8.  The genomic complexity of primary human prostate cancer.

Authors:  Michael F Berger; Michael S Lawrence; Francesca Demichelis; Yotam Drier; Kristian Cibulskis; Andrey Y Sivachenko; Andrea Sboner; Raquel Esgueva; Dorothee Pflueger; Carrie Sougnez; Robert Onofrio; Scott L Carter; Kyung Park; Lukas Habegger; Lauren Ambrogio; Timothy Fennell; Melissa Parkin; Gordon Saksena; Douglas Voet; Alex H Ramos; Trevor J Pugh; Jane Wilkinson; Sheila Fisher; Wendy Winckler; Scott Mahan; Kristin Ardlie; Jennifer Baldwin; Jonathan W Simons; Naoki Kitabayashi; Theresa Y MacDonald; Philip W Kantoff; Lynda Chin; Stacey B Gabriel; Mark B Gerstein; Todd R Golub; Matthew Meyerson; Ashutosh Tewari; Eric S Lander; Gad Getz; Mark A Rubin; Levi A Garraway
Journal:  Nature       Date:  2011-02-10       Impact factor: 49.962

9.  The variant call format and VCFtools.

Authors:  Petr Danecek; Adam Auton; Goncalo Abecasis; Cornelis A Albers; Eric Banks; Mark A DePristo; Robert E Handsaker; Gerton Lunter; Gabor T Marth; Stephen T Sherry; Gilean McVean; Richard Durbin
Journal:  Bioinformatics       Date:  2011-06-07       Impact factor: 6.937

10.  Sensitive detection of somatic point mutations in impure and heterogeneous cancer samples.

Authors:  Kristian Cibulskis; Michael S Lawrence; Scott L Carter; Andrey Sivachenko; David Jaffe; Carrie Sougnez; Stacey Gabriel; Matthew Meyerson; Eric S Lander; Gad Getz
Journal:  Nat Biotechnol       Date:  2013-02-10       Impact factor: 54.908

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  30 in total

1.  iPSCs and fibroblast subclones from the same fibroblast population contain comparable levels of sequence variations.

Authors:  Erika M Kwon; John P Connelly; Nancy F Hansen; Frank X Donovan; Thomas Winkler; Brian W Davis; Halah Alkadi; Settara C Chandrasekharappa; Cynthia E Dunbar; James C Mullikin; Paul Liu
Journal:  Proc Natl Acad Sci U S A       Date:  2017-02-06       Impact factor: 11.205

Review 2.  Somatic mutation load and spectra: A record of DNA damage and repair in healthy human cells.

Authors:  Natalie Saini; Dmitry A Gordenin
Journal:  Environ Mol Mutagen       Date:  2018-08-27       Impact factor: 3.216

3.  An improved understanding of cancer genomics through massively parallel sequencing.

Authors:  Jamie K Teer
Journal:  Transl Cancer Res       Date:  2014-06       Impact factor: 1.241

4.  Comparative clinical and genomic analysis of neurofibromatosis type 2-associated cranial and spinal meningiomas.

Authors:  Alexander Pemov; Ramita Dewan; Nancy F Hansen; Settara C Chandrasekharappa; Abhik Ray-Chaudhury; Kristine Jones; Wen Luo; John D Heiss; James C Mullikin; Prashant Chittiboina; Douglas R Stewart; Ashok R Asthagiri
Journal:  Sci Rep       Date:  2020-07-28       Impact factor: 4.379

5.  Somatic Mutations Increase Hepatic Clonal Fitness and Regeneration in Chronic Liver Disease.

Authors:  Min Zhu; Tianshi Lu; Yuemeng Jia; Xin Luo; Purva Gopal; Lin Li; Mobolaji Odewole; Veronica Renteria; Amit G Singal; Younghoon Jang; Kai Ge; Sam C Wang; Mahsa Sorouri; Justin R Parekh; Malcolm P MacConmara; Adam C Yopp; Tao Wang; Hao Zhu
Journal:  Cell       Date:  2019-04-04       Impact factor: 41.582

6.  Somatic and Germline Variant Calling from Next-Generation Sequencing Data.

Authors:  Ti-Cheng Chang; Ke Xu; Zhongshan Cheng; Gang Wu
Journal:  Adv Exp Med Biol       Date:  2022       Impact factor: 2.622

7.  Germline and sporadic mTOR pathway mutations in low-grade oncocytic tumor of the kidney.

Authors:  Payal Kapur; Ming Gao; Hua Zhong; Suneetha Chintalapati; Midori Mitui; Spencer D Barnes; Qinbo Zhou; Jeffrey Miyata; Deyssy Carrillo; Venkat S Malladi; Dinesh Rakheja; Ivan Pedrosa; Lin Xu; Lisa Kinch; James Brugarolas
Journal:  Mod Pathol       Date:  2021-09-20       Impact factor: 8.209

8.  Uncovering Biological Factors That Regulate Hepatocellular Carcinoma Growth Using Patient-Derived Xenograft Assays.

Authors:  Min Zhu; Lin Li; Tianshi Lu; Hyesun Yoo; Ji Zhu; Purva Gopal; Sam C Wang; Matthew R Porembka; Nicole E Rich; Sofia Kagan; Mobolaji Odewole; Veronica Renteria; Akbar K Waljee; Tao Wang; Amit G Singal; Adam C Yopp; Hao Zhu
Journal:  Hepatology       Date:  2020-09-02       Impact factor: 17.425

9.  Pancreatic tropism of metastatic renal cell carcinoma.

Authors:  Nirmish Singla; Zhiqun Xie; Ze Zhang; Ming Gao; Qurratulain Yousuf; Oreoluwa Onabolu; Tiffani McKenzie; Vanina Toffessi Tcheuyap; Yuanqing Ma; Jacob Choi; Renee McKay; Alana Christie; Oscar Reig Torras; Isaac A Bowman; Vitaly Margulis; Ivan Pedrosa; Christopher Przybycin; Tao Wang; Payal Kapur; Brian Rini; James Brugarolas
Journal:  JCI Insight       Date:  2020-04-09

10.  ExScalibur: A High-Performance Cloud-Enabled Suite for Whole Exome Germline and Somatic Mutation Identification.

Authors:  Riyue Bao; Kyle Hernandez; Lei Huang; Wenjun Kang; Elizabeth Bartom; Kenan Onel; Samuel Volchenboum; Jorge Andrade
Journal:  PLoS One       Date:  2015-08-13       Impact factor: 3.240

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