Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Andrew N Bortvin"'
Autor:
Sara A Carioscia, Kathryn J Weaver, Andrew N Bortvin, Hao Pan, Daniel Ariad, Avery Davis Bell, Rajiv C McCoy
Publikováno v:
eLife, Vol 11 (2022)
Recently published single-cell sequencing data from individual human sperm (n=41,189; 969–3377 cells from each of 25 donors) offer an opportunity to investigate questions of inheritance with improved statistical power, but require new methods tailo
Externí odkaz:
https://doaj.org/article/6bafe8d47ed24f0ea0160075e2505c8f
Autor:
Stephanie M Yan, Rachel M Sherman, Dylan J Taylor, Divya R Nair, Andrew N Bortvin, Michael C Schatz, Rajiv C McCoy
Publikováno v:
eLife, Vol 10 (2021)
Large genomic insertions and deletions are a potent source of functional variation, but are challenging to resolve with short-read sequencing, limiting knowledge of the role of such structural variants (SVs) in human evolution. Here, we used a graph-
Externí odkaz:
https://doaj.org/article/b54707afd69748fd9569c8f3c10b6a1f
Autor:
Kathryn J Weaver, Sara A Carioscia, Andrew N Bortvin, Hao Pan, Daniel Ariad, Avery Davis Bell, Rajiv C McCoy
Publikováno v:
eLife. 11
Recently published single-cell sequencing data from individual human sperm (n=41,189; 969–3377 cells from each of 25 donors) offer an opportunity to investigate questions of inheritance with improved statistical power, but require new methods tailo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e14ce084b00bf4e17241344c569ad701
https://doi.org/10.7554/elife.76383
https://doi.org/10.7554/elife.76383
Autor:
Kathryn Weaver, Rajiv C. McCoy, Daniel Ariad, Andrew N. Bortvin, Sara A. Carioscia, Avery Davis Bell
Mendel’s Law of Segregation states that the offspring of a diploid, heterozygous parent will inherit either allele with equal probability. While the vast majority of loci adhere to this rule, research in model and non-model organisms has uncovered
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d29e9133f34dbcd4238ef5870115b530
https://doi.org/10.1101/2021.11.19.469261
https://doi.org/10.1101/2021.11.19.469261
Autor:
Divya Nair, Michael C. Schatz, Rachel M. Sherman, Stephanie M Yan, Dylan J. Taylor, Andrew N. Bortvin, Rajiv C. McCoy
Publikováno v:
eLife, Vol 10 (2021)
eLife
eLife
Large genomic insertions, deletions, and inversions are a potent source of functional and fitness-altering variation, but are challenging to resolve with short-read DNA sequencing alone. While recent long-read sequencing technologies have greatly exp
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1f069c572ac6ca0ecfb15cc9148ea5ae
https://elifesciences.org/articles/67615
https://elifesciences.org/articles/67615