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cocchi.e89
cocchi.e89
Reputation:
300 (Trusted)
Joined:
7.7 years ago
Last seen:
3.6 years ago
Location:
United States
Google Scholar:
7mj6LfsAAAAJ
Twitter:
cocchi_enrico
Latest posts by user
4 votes
0 replies
1.4K views
Tool: Visual analysis of VCF files
vcf visual-analysis
updated by Ram 4.5K • | written by cocchi.e89 30
0 votes
0 replies
0 views
Answer: Answer: Plot number of mutations in each cancer type in VCF files?
written by cocchi.e89 30
0 votes
0 replies
0 views
Answer: Answer: Mutational landscape plot from VCF files
written by cocchi.e89 30
0 votes
0 replies
0 views
Answer: Answer: plotting AF in vcf files
written by cocchi.e89 30
1 vote
0 replies
0 views
Answer: Answer: Making nice plots based on the different metrics from VCF file
written by cocchi.e89 30
0 votes
0 replies
0 views
Comment: Comment: hg38 low-quality site BED file
written by cocchi.e89 30
0 votes
1 reply
0 views
Comment: Comment: hg38 low-quality site BED file
written by cocchi.e89 30
0 votes
1 reply
0 views
Comment: Comment: hg38 low-quality site BED file
written by cocchi.e89 30
1 vote
8 replies
3.5K views
hg38 low-quality site BED file
human low-quality-site bed hg38
written by cocchi.e89 30
1 vote
1 reply
1.7K views
gene pLI score
gene loss-of-function pli
updated by LChart 518 • | written by cocchi.e89 30
0 votes
0 replies
777 views
mosaic loss of chromosome - bioinformatics score
gatk chromosome cnv loss mosaic
written by cocchi.e89 30
0 votes
1 reply
1.2K views
why Mutect2 calls some germline variants as somatic ones?
somatic germline haplotypecaller mutect2
updated by Shred 163 • | written by cocchi.e89 30
0 votes
1 reply
1.0K views
Genome variants - regional distribution analysis
genome human variants distribution
updated by liorglic 150 • | written by cocchi.e89 30
0 votes
0 replies
875 views
updated in-silico scoring system for missense variants
pathogenicity missense in-silico
written by cocchi.e89 30
1 vote
1 reply
1.9K views
GenomicsDBImport from Mutect2 output
mutect2 genomicsdbimport somatic vcf gatk
updated by sure 11 • | written by cocchi.e89 30
0 votes
0 replies
0 views
Comment: Comment: GATK genomicsDBimport intervals for WGS
written by cocchi.e89 30
0 votes
0 replies
846 views
average variants number human WGS
variant wgs snp indel
written by cocchi.e89 30
0 votes
1 reply
0 views
Comment: Comment: GATK SelectVariants consider spanning/overlapping deletions as SNP
written by cocchi.e89 30
0 votes
5 replies
2.7K views
GATK SelectVariants consider spanning/overlapping deletions as SNP
selectvariants snp gatk indel
updated by jon.klonowski 21 • | written by cocchi.e89 30
1 vote
0 replies
1.7K views
germline vs somatic CNV GATK calling
cnv germline somatic gatk wgs
written by cocchi.e89 30
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