| Id: | hg19/scores/Linsight |
| Type: | position_score |
| Version: | 0 |
| Summary: |
LINSIGHT score quantifies the likelihood of negative selection on noncoding sites. |
| Description: |
LINSIGHT improves the prediction of noncoding nucleotide sites at which mutations are likely to have deleterious fitness consequences, and which, therefore, are likely to be phenotypically important. LINSIGHT combines a generalized linear model for functional genomic data with a probabilistic model of molecular evolution. Huang, YF., Gulko, B. & Siepel, A. Fast, scalable prediction of deleterious noncoding variants from functional and population genomic data. Nat Genet 49, 618-624 (2017). https://doi.org/10.1038/ng.3810 TODO |
| Labels: |
|
| ID | Type | Default annotation | Description | Histogram | Range |
|---|---|---|---|---|---|
| Linsight | float |
linsight |
The LINSIGHT score measures the probability of negative selection on noncoding
sites.
Small values desc: negative selection is less likely
Large values desc: negative selection is more likely
|
 |
[0.033, 0.995] |
| Filename | Size | md5 |
|---|---|---|
| Linsight.bed.gz | 1.35 GB | a92973c6f355df17cf74f29888dcaa46 |
| Linsight.bed.gz.dvc | 89.0 B | a6f44efbe7c9bab704b196f04e141419 |
| Linsight.bed.gz.tbi | 810.83 KB | 429ff3098769c12759f054680a917c6a |
| Linsight.bed.gz.tbi.dvc | 89.0 B | caa1065db1ccbcb86c3b37fe182dd9c5 |
| genomic_resource.yaml | 1.44 KB | 022847d6e5bb395c868b1f4ecc48aa66 |
| statistics/ |