{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,4,7]],"date-time":"2026-04-07T00:18:38Z","timestamp":1775521118777,"version":"3.50.1"},"reference-count":5,"publisher":"Oxford University Press (OUP)","issue":"19","funder":[{"DOI":"10.13039\/100000051","name":"National Human Genome Research Institute","doi-asserted-by":"publisher","award":["R01-HG006677"],"award-info":[{"award-number":["R01-HG006677"]}],"id":[{"id":"10.13039\/100000051","id-type":"DOI","asserted-by":"publisher"}]},{"DOI":"10.13039\/100000001","name":"National Science Foundation","doi-asserted-by":"publisher","award":["DBI-1350041"],"award-info":[{"award-number":["DBI-1350041"]}],"id":[{"id":"10.13039\/100000001","id-type":"DOI","asserted-by":"publisher"}]}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":[],"published-print":{"date-parts":[[2016,10,1]]},"abstract":"<jats:title>Abstract<\/jats:title>\n                  <jats:p>Summary: Assemblytics is a web app for detecting and analyzing variants from a de novo genome assembly aligned to a reference genome. It incorporates a unique anchor filtering approach to increase robustness to repetitive elements, and identifies six classes of variants based on their distinct alignment signatures. Assemblytics can be applied both to comparing aberrant genomes, such as human cancers, to a reference, or to identify differences between related species. Multiple interactive visualizations enable in-depth explorations of the genomic distributions of variants.<\/jats:p>\n                  <jats:p>Availability and Implementation: \u00a0http:\/\/assemblytics.com, https:\/\/github.com\/marianattestad\/assemblytics<\/jats:p>\n                  <jats:p>Contact: \u00a0mnattest@cshl.edu<\/jats:p>\n                  <jats:p>Supplementary information: \u00a0Supplementary data are available at Bioinformatics online.<\/jats:p>","DOI":"10.1093\/bioinformatics\/btw369","type":"journal-article","created":{"date-parts":[[2016,6,18]],"date-time":"2016-06-18T20:18:20Z","timestamp":1466281100000},"page":"3021-3023","source":"Crossref","is-referenced-by-count":334,"title":["Assemblytics: a web analytics tool for the detection of variants from an assembly"],"prefix":"10.1093","volume":"32","author":[{"given":"Maria","family":"Nattestad","sequence":"first","affiliation":[{"name":"1 Cold Spring Harbor Laboratory, Simons Center for Quantitative Biology, Cold Spring Harbor, NY, USA and"}]},{"given":"Michael C.","family":"Schatz","sequence":"additional","affiliation":[{"name":"1 Cold Spring Harbor Laboratory, Simons Center for Quantitative Biology, Cold Spring Harbor, NY, USA and"},{"name":"2 Department of Computer Science, Johns Hopkins University, Baltimore, MD, USA"}]}],"member":"286","published-online":{"date-parts":[[2016,6,17]]},"reference":[{"key":"2023020201172908300_btw369-B1","doi-asserted-by":"crossref","first-page":"623","DOI":"10.1038\/nbt.3238","article-title":"Assembling large genomes with single-molecule sequencing and locality-sensitive hashing","volume":"33","author":"Berlin","year":"2015","journal-title":"Nat. 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