Show simple item record

dc.identifier.urihttp://hdl.handle.net/11401/76484
dc.description.sponsorshipThis work is sponsored by the Stony Brook University Graduate School in compliance with the requirements for completion of degree.en_US
dc.formatMonograph
dc.format.mediumElectronic Resourceen_US
dc.language.isoen_US
dc.publisherThe Graduate School, Stony Brook University: Stony Brook, NY.
dc.typeDissertation
dcterms.abstractIntra-tumoral genetic heterogeneity has long been recognized, yet remains poorly understood. This has primarily been due to the lack of sensitive technologies to measure it. Genome wide analysis at the level of single cells has recently emerged as a powerful tool to dissect cancer genome heterogeneity. However, to be truly transformative, single cell approaches must accommodate the analysis of large numbers of single cells. Here, using integrative informatics and molecular biology approaches this study presents a robust, low-cost, and high-throughput method to retrieve the genome-wide copy number landscape of hundreds of single cancer cells. Application of the method to human cancer cell lines and clinical cancer tissue illustrates the underlying genetic heterogeneity present in both and further reveals mosaicism of chromosomal amplifications in clinical cancer samples. The capacity of the method to facilitate the rapid profiling of hundreds and thousands of single cell genomes is bound to illuminate the biology of intra-tumoral heterogeneity.
dcterms.available2017-09-20T16:50:23Z
dcterms.contributorShroyer, Kennethen_US
dcterms.contributorHicks, Jamesen_US
dcterms.contributorJu, Jingfangen_US
dcterms.contributorOffit, Kennethen_US
dcterms.contributorKrasnitz, Alexander.en_US
dcterms.creatorBaslan, Taimour
dcterms.dateAccepted2017-09-20T16:50:23Z
dcterms.dateSubmitted2017-09-20T16:50:23Z
dcterms.descriptionDepartment of Molecular and Cellular Biology.en_US
dcterms.extent99 pg.en_US
dcterms.formatApplication/PDFen_US
dcterms.formatMonograph
dcterms.identifierhttp://hdl.handle.net/11401/76484
dcterms.issued2014-12-01
dcterms.languageen_US
dcterms.provenanceMade available in DSpace on 2017-09-20T16:50:23Z (GMT). No. of bitstreams: 1 Baslan_grad.sunysb_0771E_12105.pdf: 29921219 bytes, checksum: e677504493d2616f6f5dc7193ae08c57 (MD5) Previous issue date: 1en
dcterms.publisherThe Graduate School, Stony Brook University: Stony Brook, NY.
dcterms.subjectCopy Number Variation, Genome Evolution, Intra-Tumoral Heterogeneity, Multiplexing, Sequencing, Single Cell
dcterms.subjectGenetics
dcterms.titleHigh-Throughput Single-Cell Copy Number Profiling for Cancer Heterogeneity Analysis
dcterms.typeDissertation


Files in this item

Thumbnail

This item appears in the following Collection(s)

Show simple item record