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pro vyhledávání: '"Andrew Fujikawa"'
Autor:
Roummel F. Marcia, Katharine Sanderson, Jonathan Sahagun, Mario Banuelos, Rubi Almanza, Andrew Fujikawa, Melissa Spence, Suzanne Sindi, Lasith Adhikari
Publikováno v:
MeMeA
Recent research suggests an overwhelming proportion of humans have genomic structural variants (SVs): rearrangements of regions in the genome such as inversions, insertions, deletions and duplications. The standard approach to detecting SVs in an unk
Autor:
Andrew Fujikawa, Lasith Adhikari, Jonathan Sahagun, Rubi Almanza, Melissa Spence, Mario Banuelos, Suzanne Sindi, Roummel F. Marcia, Katharine Sanderson
Publikováno v:
MeMeA
Structural variants (SVs) - such as duplications, deletions and inversions - are rearrangements of an individual's genome relative to a given reference. The common method for detection of SVs is to sequence fragments from an individual's genome, map