Zobrazeno 1 - 10
of 37
pro vyhledávání: '"Melissa Spence"'
Autor:
Teresa Naseba Marsh, Carol Eshakakogan, Joseph K. Eibl, Melissa Spence, Kristen A. Morin, Patrick Oghene, Aidan Goertzen, Farah Tahsin, Graham J. Gauthier, Chief Dean Sayers, Chief Alan Ozawanimke, Chief Brent Bissaillion, David C. Marsh
Background: Indigenous peoples with substance use disorders (SUD) and intergenerational trauma (IGT) have a variety of needs across the range of symptom severity and the challenging dual disorder (1). To address these needs, a continuum of holistic c
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::905d06a2dcd726e4f6c8e69490a82857
https://doi.org/10.21203/rs.3.rs-2034604/v1
https://doi.org/10.21203/rs.3.rs-2034604/v1
Publikováno v:
EUSIPCO
Structural variants (SVs) are rearrangements in the DNA sequence of members within the same species. Detecting SVs is challenging because most approaches suffer from high-false positive rates. In this work, we improve the accuracy of SV detection by
Publikováno v:
BIBM
Genomic variation shared by members of the same species that are longer than a single nucleotide are commonly called structural variants (SVs). Though relatively rare, they represent an increasingly important class of variation as SVs have been assoc
Publikováno v:
MeMeA
Genomic variation shared by members of the same species that are longer than a single nucleotide are commonly called structural variants (SVs). Though relatively rare, they represent an increasingly important class of variation as SVs have been assoc
Publikováno v:
Methods (San Diego, Calif.). 173
Structural variants (SVs) are a class of genomic variation shared by members of the same species. Though relatively rare, they represent an increasingly important class of variation, as SVs have been associated with diseases and susceptibility to som
Publikováno v:
BIBM
Genomic variation shared by members of the same species that are longer than a single nucleotide are commonly called structural variants (SVs). Though relatively rare, they represent an increasingly important class of variation as SVs have been assoc
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
Publikováno v:
Seminars in Dialysis. 26:164-168
Access to education, communication, and support is essential for achieving and maintaining a skilled healthcare workforce. Delivering affordable and accessible continuing education for healthcare providers in rural, remote, and isolated First Nation
Publikováno v:
Seminars in dialysis. 26(2)
Access to education, communication, and support is essential for achieving and maintaining a skilled healthcare workforce. Delivering affordable and accessible continuing education for healthcare providers in rural, remote, and isolated First Nation