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AutoCSA, an algorithm for high throughput DNA sequence variant detection in cancer genomes
The undertaking of large-scale DNA sequencing screens for somatic variants in human cancers requires accurate and rapid processing of traces for variants. Due to their often aneuploid nature and admixed normal tissue, heterozygous variants found in primary cancers are often subtle and difficult to d...
Autores principales: | , , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
2007
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5947781/ https://www.ncbi.nlm.nih.gov/pubmed/17485433 http://dx.doi.org/10.1093/bioinformatics/btm152 |
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author | Dicks, E. Teague, J. W. Stephens, P. Raine, K. Yates, A. Mattocks, C. Tarpey, P. Butler, A. Menzies, A. Richardson, D. Jenkinson, A. Davies, H. Edkins, S. Forbes, S. Gray, K. Greenman, C. Shepherd, R. Stratton, M. R. Futreal, P. A. Wooster, R. |
author_facet | Dicks, E. Teague, J. W. Stephens, P. Raine, K. Yates, A. Mattocks, C. Tarpey, P. Butler, A. Menzies, A. Richardson, D. Jenkinson, A. Davies, H. Edkins, S. Forbes, S. Gray, K. Greenman, C. Shepherd, R. Stratton, M. R. Futreal, P. A. Wooster, R. |
author_sort | Dicks, E. |
collection | PubMed |
description | The undertaking of large-scale DNA sequencing screens for somatic variants in human cancers requires accurate and rapid processing of traces for variants. Due to their often aneuploid nature and admixed normal tissue, heterozygous variants found in primary cancers are often subtle and difficult to detect. To address these issues, we have developed a mutation detection algorithm, AutoCSA, specifically optimized for the high throughput screening of cancer samples. |
format | Online Article Text |
id | pubmed-5947781 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2007 |
record_format | MEDLINE/PubMed |
spelling | pubmed-59477812018-05-11 AutoCSA, an algorithm for high throughput DNA sequence variant detection in cancer genomes Dicks, E. Teague, J. W. Stephens, P. Raine, K. Yates, A. Mattocks, C. Tarpey, P. Butler, A. Menzies, A. Richardson, D. Jenkinson, A. Davies, H. Edkins, S. Forbes, S. Gray, K. Greenman, C. Shepherd, R. Stratton, M. R. Futreal, P. A. Wooster, R. Bioinformatics Article The undertaking of large-scale DNA sequencing screens for somatic variants in human cancers requires accurate and rapid processing of traces for variants. Due to their often aneuploid nature and admixed normal tissue, heterozygous variants found in primary cancers are often subtle and difficult to detect. To address these issues, we have developed a mutation detection algorithm, AutoCSA, specifically optimized for the high throughput screening of cancer samples. 2007-05-07 2007-07-01 /pmc/articles/PMC5947781/ /pubmed/17485433 http://dx.doi.org/10.1093/bioinformatics/btm152 Text en http://creativecommons.org/licenses/by-nc/2.0/uk/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/2.0/uk/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Article Dicks, E. Teague, J. W. Stephens, P. Raine, K. Yates, A. Mattocks, C. Tarpey, P. Butler, A. Menzies, A. Richardson, D. Jenkinson, A. Davies, H. Edkins, S. Forbes, S. Gray, K. Greenman, C. Shepherd, R. Stratton, M. R. Futreal, P. A. Wooster, R. AutoCSA, an algorithm for high throughput DNA sequence variant detection in cancer genomes |
title | AutoCSA, an algorithm for high throughput DNA sequence variant detection in cancer genomes |
title_full | AutoCSA, an algorithm for high throughput DNA sequence variant detection in cancer genomes |
title_fullStr | AutoCSA, an algorithm for high throughput DNA sequence variant detection in cancer genomes |
title_full_unstemmed | AutoCSA, an algorithm for high throughput DNA sequence variant detection in cancer genomes |
title_short | AutoCSA, an algorithm for high throughput DNA sequence variant detection in cancer genomes |
title_sort | autocsa, an algorithm for high throughput dna sequence variant detection in cancer genomes |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5947781/ https://www.ncbi.nlm.nih.gov/pubmed/17485433 http://dx.doi.org/10.1093/bioinformatics/btm152 |
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