Resource

Id:	hg38/scores/CADD_v1.6
Type:	allele_score
Version:	0
Summary:
Description:
Labels:	reference_genome: hg38/genomes/GRCh38-hg38

Scores

ID	Type	Default annotation	Description	Histogram	Range
cadd_raw	float	cadd_raw	CADD raw score for functional prediction of a SNP. The larger the score the more likely the SNP has damaging effect Small values desc: less damaging Large values desc: more damaging		[-19.812, 25.029]
cadd_phred	float	cadd_phred	CADD phred-like score. This is phred-like rank score based on whole genome CADD raw scores. The larger the score the more likely the SNP has damaging effect. Small values desc: less damaging Large values desc: more damaging		[0.000, 99.000]

Filename	Size	md5
genomic_resource.yaml	2.06 KB	a20512bd881b1fd20ec2669c9e99f671
whole_genome_SNVs.tsv.gz	80.65 GB	faaa80ef3948cf44e56a3629a90cdaaa
whole_genome_SNVs.tsv.gz.dvc	99.0 B	20780cfd6231c84d36dcb6ecdc526b42
whole_genome_SNVs.tsv.gz.sha256	91.0 B	e68d5fd28400e4251e5b6f624ac7130c
whole_genome_SNVs.tsv.gz.tbi	2.63 MB	4e5aeff342ecdb498377aa186e4f8d84
whole_genome_SNVs.tsv.gz.tbi.dvc	99.0 B	ca6c099b2aa7498561afc021032c049d
whole_genome_SNVs.tsv.gz.tbi.sha256	95.0 B	aaf6836d60b8ead14fc0aab1bc9ba097
statistics/