Literature DB >> 18355774

SNP arrays in heterogeneous tissue: highly accurate collection of both germline and somatic genetic information from unpaired single tumor samples.

Guillaume Assié1, Thomas LaFramboise, Petra Platzer, Jérôme Bertherat, Constantine A Stratakis, Charis Eng.   

Abstract

SNP arrays provide reliable genotypes and can detect chromosomal aberrations at a high resolution. However, tissue heterogeneity is currently a major limitation for somatic tissue analysis. We have developed SOMATICs, an original program for accurate analysis of heterogeneous tissue samples. Fifty-four samples (42 tumors and 12 normal tissues) were processed through Illumina Beadarrays and then analyzed with SOMATICs. We demonstrate that tissue heterogeneity-related limitations not only can be overcome but can also be turned into an advantage. First, admixture of normal cells with tumor can be used as an internal reference, thereby enabling highly sensitive detection of somatic deletions without having corresponding normal tissue. Second, the presence of normal cells allows for discrimination of somatic from germline aberrations, and the proportion of cells in the tissue sample that are harboring the somatic events can be assessed. Third, relatively early versus late somatic events can also be distinguished, assuming that late events occur only in subsets of cancer cells. Finally, admixture by normal cells allows inference of germline genotypes from a cancer sample. All this information can be obtained from any cancer sample containing a proportion of 40-75% of cancer cells. SOMATICs is a ready-to-use open-source program that integrates all of these features into a simple format, comprehensively describing each chromosomal event.

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Year:  2008        PMID: 18355774      PMCID: PMC2427213          DOI: 10.1016/j.ajhg.2008.01.012

Source DB:  PubMed          Journal:  Am J Hum Genet        ISSN: 0002-9297            Impact factor:   11.025


  36 in total

1.  dChipSNP: significance curve and clustering of SNP-array-based loss-of-heterozygosity data.

Authors:  Ming Lin; Lee-Jen Wei; William R Sellers; Marshall Lieberfarb; Wing Hung Wong; Cheng Li
Journal:  Bioinformatics       Date:  2004-02-10       Impact factor: 6.937

2.  Genomewide single nucleotide polymorphism microarray mapping in basal cell carcinomas unveils uniparental disomy as a key somatic event.

Authors:  Muy-Teck Teh; Diana Blaydon; Tracy Chaplin; Nicola J Foot; Spyros Skoulakis; Manoj Raghavan; Catherine A Harwood; Charlotte M Proby; Michael P Philpott; Bryan D Young; David P Kelsell
Journal:  Cancer Res       Date:  2005-10-01       Impact factor: 12.701

3.  Loss of heterozygosity in childhood acute lymphoblastic leukemia detected by genome-wide microarray single nucleotide polymorphism analysis.

Authors:  Julie A E Irving; Lisa Bloodworth; Nick P Bown; Marian C Case; Linda A Hogarth; Andrew G Hall
Journal:  Cancer Res       Date:  2005-04-15       Impact factor: 12.701

4.  High-density single nucleotide polymorphism array defines novel stage and location-dependent allelic imbalances in human bladder tumors.

Authors:  Karen Koed; Carsten Wiuf; Lise-Lotte Christensen; Friedrik P Wikman; Karsten Zieger; Klaus Møller; Hans von der Maase; Torben F Orntoft
Journal:  Cancer Res       Date:  2005-01-01       Impact factor: 12.701

5.  A robust algorithm for copy number detection using high-density oligonucleotide single nucleotide polymorphism genotyping arrays.

Authors:  Yasuhito Nannya; Masashi Sanada; Kumi Nakazaki; Noriko Hosoya; Lili Wang; Akira Hangaishi; Mineo Kurokawa; Shigeru Chiba; Dione K Bailey; Giulia C Kennedy; Seishi Ogawa
Journal:  Cancer Res       Date:  2005-07-15       Impact factor: 12.701

6.  Combined array-comparative genomic hybridization and single-nucleotide polymorphism-loss of heterozygosity analysis reveals complex changes and multiple forms of chromosomal instability in colorectal cancers.

Authors:  Michelle Gaasenbeek; Kimberley Howarth; Andrew J Rowan; Patricia A Gorman; Angela Jones; Tracy Chaplin; Ying Liu; David Bicknell; Eleanor J Davison; Heike Fiegler; Nigel P Carter; Rebecca R Roylance; Ian P M Tomlinson
Journal:  Cancer Res       Date:  2006-04-01       Impact factor: 12.701

7.  Clinical and molecular genetics of patients with the Carney-Stratakis syndrome and germline mutations of the genes coding for the succinate dehydrogenase subunits SDHB, SDHC, and SDHD.

Authors:  Barbara Pasini; Sarah R McWhinney; Thalia Bei; Ludmila Matyakhina; Sotirios Stergiopoulos; Michael Muchow; Sosipatros A Boikos; Barbara Ferrando; Karel Pacak; Guillaume Assie; Eric Baudin; Agnes Chompret; Jay W Ellison; Jean-Jacques Briere; Pierre Rustin; Anne-Paule Gimenez-Roqueplo; Charis Eng; J Aidan Carney; Constantine A Stratakis
Journal:  Eur J Hum Genet       Date:  2007-08-01       Impact factor: 4.246

8.  BeadArray technology: enabling an accurate, cost-effective approach to high-throughput genotyping.

Authors:  Arnold Oliphant; David L Barker; John R Stuelpnagel; Mark S Chee
Journal:  Biotechniques       Date:  2002-06       Impact factor: 1.993

9.  Genome-wide detection of LOH in prostate cancer using human SNP microarray technology.

Authors:  Catherine I Dumur; Chavaboon Dechsukhum; Joy L Ware; Stacey S Cofield; Al M Best; David S Wilkinson; Carleton T Garrett; Andrea Ferreira-Gonzalez
Journal:  Genomics       Date:  2003-03       Impact factor: 5.736

10.  CARAT: a novel method for allelic detection of DNA copy number changes using high density oligonucleotide arrays.

Authors:  Jing Huang; Wen Wei; Joyce Chen; Jane Zhang; Guoying Liu; Xiaojun Di; Rui Mei; Shumpei Ishikawa; Hiroyuki Aburatani; Keith W Jones; Michael H Shapero
Journal:  BMC Bioinformatics       Date:  2006-02-21       Impact factor: 3.169

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  31 in total

1.  BACOM: in silico detection of genomic deletion types and correction of normal cell contamination in copy number data.

Authors:  Guoqiang Yu; Bai Zhang; G Steven Bova; Jianfeng Xu; Ie-Ming Shih; Yue Wang
Journal:  Bioinformatics       Date:  2011-04-15       Impact factor: 6.937

2.  Parent-specific copy number in paired tumor-normal studies using circular binary segmentation.

Authors:  Adam B Olshen; Henrik Bengtsson; Pierre Neuvial; Paul T Spellman; Richard A Olshen; Venkatraman E Seshan
Journal:  Bioinformatics       Date:  2011-06-11       Impact factor: 6.937

3.  ARMC5 mutations in macronodular adrenal hyperplasia with Cushing's syndrome.

Authors:  Guillaume Assié; Rossella Libé; Stéphanie Espiard; Marthe Rizk-Rabin; Anne Guimier; Windy Luscap; Olivia Barreau; Lucile Lefèvre; Mathilde Sibony; Laurence Guignat; Stéphanie Rodriguez; Karine Perlemoine; Fernande René-Corail; Franck Letourneur; Bilal Trabulsi; Alix Poussier; Nathalie Chabbert-Buffet; Françoise Borson-Chazot; Lionel Groussin; Xavier Bertagna; Constantine A Stratakis; Bruno Ragazzon; Jérôme Bertherat
Journal:  N Engl J Med       Date:  2013-11-28       Impact factor: 91.245

4.  MixHMM: inferring copy number variation and allelic imbalance using SNP arrays and tumor samples mixed with stromal cells.

Authors:  Zongzhi Liu; Ao Li; Vincent Schulz; Min Chen; David Tuck
Journal:  PLoS One       Date:  2010-06-01       Impact factor: 3.240

5.  Conditional random pattern model for copy number aberration detection.

Authors:  Fuhai Li; Xiaobo Zhou; Wanting Huang; Chung-Che Chang; Stephen T C Wong
Journal:  BMC Bioinformatics       Date:  2010-04-22       Impact factor: 3.169

6.  TumorBoost: normalization of allele-specific tumor copy numbers from a single pair of tumor-normal genotyping microarrays.

Authors:  Henrik Bengtsson; Pierre Neuvial; Terence P Speed
Journal:  BMC Bioinformatics       Date:  2010-05-12       Impact factor: 3.169

7.  An integrated Bayesian analysis of LOH and copy number data.

Authors:  Paola M V Rancoita; Marcus Hutter; Francesco Bertoni; Ivo Kwee
Journal:  BMC Bioinformatics       Date:  2010-06-15       Impact factor: 3.169

Review 8.  cAMP/PKA signaling defects in tumors: genetics and tissue-specific pluripotential cell-derived lesions in human and mouse.

Authors:  Constantine A Stratakis
Journal:  Mol Cell Endocrinol       Date:  2013-02-26       Impact factor: 4.102

9.  Single nucleotide polymorphism arrays: a decade of biological, computational and technological advances.

Authors:  Thomas LaFramboise
Journal:  Nucleic Acids Res       Date:  2009-07-01       Impact factor: 16.971

10.  Genome Alteration Print (GAP): a tool to visualize and mine complex cancer genomic profiles obtained by SNP arrays.

Authors:  Tatiana Popova; Elodie Manié; Dominique Stoppa-Lyonnet; Guillem Rigaill; Emmanuel Barillot; Marc Henri Stern
Journal:  Genome Biol       Date:  2009-11-11       Impact factor: 13.583

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