<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Bishop MR</submitter><funding>Auburn University Research Initiative in Cancer</funding><funding>Auburn University Cellular and Molecular Biosciences Peaks of Excellence Research Fellowship</funding><funding>Joy to Life Foundation</funding><funding>AURIC Graduate Fellowship Program</funding><funding>National Science Foundation Research Excellence for Undergraduates</funding><funding>American Association of Colleges of Pharmacy New Investigator Award</funding><pagination>e0220929</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC6695138</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>14(8)</volume><pubmed_abstract>There is a need to investigate and better understand the inherited risk of cancer to ensure that clinical applications provide more accurate assessments and management strategies. Developing research-based next-generation sequencing gene panels that not only target (present-day) clinically actionable susceptibility genes but also genes that currently lack sufficient evidence for risk as well as candidate genes, such as those in DNA repair pathways, can help aid this effort. Therefore, gene panel B.O.P. (Breast, Ovarian, and Prostate) was developed to evaluate the genetic risk of breast, ovarian and/or prostate cancer, and this manuscript serves as an introduction to B.O.P. and highlights its initial analytical validity assessment. B.O.P targets 87 genes that have been suggested, predicted,</pubmed_abstract><journal>PloS one</journal><pubmed_title>A research-based gene panel to investigate breast, ovarian and prostate cancer genetic risk.</pubmed_title><pmcid>PMC6695138</pmcid><funding_grant_id>NSF-EPS-1158862</funding_grant_id><funding_grant_id>1560115</funding_grant_id><pubmed_authors>Hetzel J</pubmed_authors><pubmed_authors>Huskey ALW</pubmed_authors><pubmed_authors>Bishop MR</pubmed_authors><pubmed_authors>Merner ND</pubmed_authors></additional><is_claimable>false</is_claimable><name>A research-based gene panel to investigate breast, ovarian and prostate cancer genetic risk.</name><description>There is a need to investigate and better understand the inherited risk of cancer to ensure that clinical applications provide more accurate assessments and management strategies. Developing research-based next-generation sequencing gene panels that not only target (present-day) clinically actionable susceptibility genes but also genes that currently lack sufficient evidence for risk as well as candidate genes, such as those in DNA repair pathways, can help aid this effort. Therefore, gene panel B.O.P. (Breast, Ovarian, and Prostate) was developed to evaluate the genetic risk of breast, ovarian and/or prostate cancer, and this manuscript serves as an introduction to B.O.P. and highlights its initial analytical validity assessment. B.O.P targets 87 genes that have been suggested, predicted,</description><dates><release>2019-01-01T00:00:00Z</release><publication>2019</publication><modification>2026-04-08T05:51:20.097Z</modification><creation>2019-08-21T07:03:11Z</creation></dates><accession>S-EPMC6695138</accession><cross_references><pubmed>31415627</pubmed><doi>10.1371/journal.pone.0220929</doi></cross_references></HashMap>