Literature DB >> 31750888

All-FIT: allele-frequency-based imputation of tumor purity from high-depth sequencing data.

Jui Wan Loh1,2,3, Caitlin Guccione1, Frances Di Clemente2, Gregory Riedlinger1,2,4, Shridar Ganesan1,2,5, Hossein Khiabanian1,2,4.   

Abstract

SUMMARY: Clinical sequencing aims to identify somatic mutations in cancer cells for accurate diagnosis and treatment. However, most widely used clinical assays lack patient-matched control DNA and additional analysis is needed to distinguish somatic and unfiltered germline variants. Such computational analyses require accurate assessment of tumor cell content in individual specimens. Histological estimates often do not corroborate with results from computational methods that are primarily designed for normal-tumor matched data and can be confounded by genomic heterogeneity and presence of sub-clonal mutations. Allele-frequency-based imputation of tumor (All-FIT) is an iterative weighted least square method to estimate specimen tumor purity based on the allele frequencies of variants detected in high-depth, targeted, clinical sequencing data. Using simulated and clinical data, we demonstrate All-FIT's accuracy and improved performance against leading computational approaches, highlighting the importance of interpreting purity estimates based on expected biology of tumors.
AVAILABILITY AND IMPLEMENTATION: Freely available at http://software.khiabanian-lab.org. SUPPLEMENTARY INFORMATION: Supplementary data are available at Bioinformatics online.
© The Author(s) 2019. Published by Oxford University Press. All rights reserved. For permissions, please e-mail: journals.permissions@oup.com.

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Year:  2020        PMID: 31750888      PMCID: PMC7141867          DOI: 10.1093/bioinformatics/btz865

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


  26 in total

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3.  Allele-specific copy number analysis of tumors.

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5.  Control-FREEC: a tool for assessing copy number and allelic content using next-generation sequencing data.

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Review 9.  Translating insights into tumor evolution to clinical practice: promises and challenges.

Authors:  Matthew W Fittall; Peter Van Loo
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10.  Clinical Actionability of Comprehensive Genomic Profiling for Management of Rare or Refractory Cancers.

Authors:  Kim M Hirshfield; Denis Tolkunov; Hua Zhong; Siraj M Ali; Mark N Stein; Susan Murphy; Hetal Vig; Alexei Vazquez; John Glod; Rebecca A Moss; Vladimir Belyi; Chang S Chan; Suzie Chen; Lauri Goodell; David Foran; Roman Yelensky; Norma A Palma; James X Sun; Vincent A Miller; Philip J Stephens; Jeffrey S Ross; Howard Kaufman; Elizabeth Poplin; Janice Mehnert; Antoinette R Tan; Joseph R Bertino; Joseph Aisner; Robert S DiPaola; Lorna Rodriguez-Rodriguez; Shridar Ganesan
Journal:  Oncologist       Date:  2016-08-26
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  2 in total

1.  Germline Testing Data Validate Inferences of Mutational Status for Variants Detected From Tumor-Only Sequencing.

Authors:  Nahed Jalloul; Israel Gomy; Samantha Stokes; Alexander Gusev; Bruce E Johnson; Neal I Lindeman; Laura Macconaill; Shridar Ganesan; Judy E Garber; Hossein Khiabanian
Journal:  JCO Precis Oncol       Date:  2021-11-17

2.  Tumor cell enrichment by tissue suspension enables detection of mutations with low variant allele frequency and estimation of germline mutations.

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  2 in total

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