 Connection
Search Results to
This is a "connection" page, showing the details of why an item matched the keywords from your search.
One or more keywords matched the following properties of
Identification of rare and common regulatory variants in pluripotent cells using population-scale transcriptomics.
| Property | Value |
|
has minor subject area list
|
Bardet-Biedl Syndrome; Calcium Channels; Cell Line; Cerebellar Ataxia; DNA Methylation; Gene Expression; Humans; Polymorphism, Single Nucleotide; Proteins; Rare Diseases; Regulatory Sequences, Nucleic Acid; Sequence Analysis, RNA; Whole Genome Sequencing
|
|
information resource reference
|
Bonder MJ, Smail C, Gloudemans MJ, Fr?sard L, Jakubosky D, D'Antonio M, Li X, Ferraro NM, Carcamo-Orive I, Mirauta B, Seaton DD, Cai N, Vakili D, Horta D, Zhao C, Zastrow DB, Bonner DE, Wheeler MT, Kilpinen H, Knowles JW, Smith EN, Frazer KA, Montgomery SB, Stegle O. Identification of rare and common regulatory variants in pluripotent cells using population-scale transcriptomics. Nat Genet. 2021 03; 53(3):313-321.
|
|
label
|
Identification of rare and common regulatory variants in pluripotent cells using population-scale transcriptomics.
|
|
|