| 0 | ℹ |
ClinMAVE: a curated database for clinical application of data from multiplexed assays of variant effect.
(academic.oup.com)
|
Nucleic Acids Research 2026-01-06 | #cancer #database #variant #mave #clinical | |
| 0 | ℹ |
scVMAP: a comprehensive platform for integrating single-cell chromatin accessibility regions with causal variants.
(academic.oup.com)
|
Nucleic Acids Research 2026-01-06 | #single-cell #regulatory #variant #genome-wide association #single-cell sequencing | |
| 0 | ℹ |
FAVOR 2.0: A reengineered functional annotation of variants online resource for interpreting genomic variation.
(academic.oup.com)
|
Nucleic Acids Research 2026-01-06 | #genomics #sequencing #annotation #variant |