Resource

Id:hg19/scores/Linsight
Type:position_score
Summary: 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
Description:

TODO
Labels:
  • reference_genome: hg19/genomes/GATK_ResourceBundle_5777_b37_phiX174

Scores

id type default annotation description histogram range
Linsight float

linsight

 The LINSIGHT score measures the probability of negative selection on noncoding sites. HISTOGRAM FOR Linsight [0.033, 0.995]

Files

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 1.36 KB f7f4192252701bf39296283b8d9c748c
statistics/