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SunRise2019
SunRise2019
Reputation:
100
Joined:
7.3 years ago
Last seen:
4.4 years ago
Location:
Germany
Latest posts by user
0 votes
1 reply
973 views
Map hg19 whole exome data to exon number by gene
whole sequencing exome mapping exon number
updated by swbarnes2 swbarnes2 • written by SunRise2019 • SunRise2019
0 votes
1 reply
1.2K views
GATK call arm level chromosome copy number variations (cnv)
cna gatk cnv
updated by vdauwera vdauwera • written by SunRise2019 • SunRise2019
0 votes
0 replies
0 views
Comment: C: Software for clinical interpretation of variants
written by SunRise2019 • SunRise2019
0 votes
1 reply
0 views
Comment: C: Software for clinical interpretation of variants
written by SunRise2019 • SunRise2019
0 votes
0 replies
742 views
DBSNPcommon for variant filtering?
variant filtering sequencing
written by SunRise2019 • SunRise2019
0 votes
4 replies
1.9K views
Software for clinical interpretation of variants
dna sequencing variant interpretation
updated by steve steve • written by SunRise2019 • SunRise2019
0 votes
1 reply
1.4K views
How to map ENSEMBL Transcript IDs to coding/non-coding/miRNA
rna-seq mapping microarray gene expression hta
updated by Biostar Biostar • written by SunRise2019 • SunRise2019
0 votes
1 reply
0 views
Comment: C: Variant filtration software
written by SunRise2019 • SunRise2019
1 vote
6 replies
5.1K views
Variant filtration software
exome
updated by Hamid Ghaedi Hamid Ghaedi • written by SunRise2019 • SunRise2019
2 votes
1 reply
2.8K views
MAFtools variant classes mapping
variants mutations
updated by Ram Ram • written by SunRise2019 • SunRise2019
7 votes
5 replies
17K views
How to interpret variant allele frequency?
vaf maf
updated by zizigolu zizigolu • written by SunRise2019 • SunRise2019
0 votes
2 replies
1.7K views
Detect gene expression signatures in own dataset
rna-seq array
updated by vj vj • written by SunRise2019 • SunRise2019
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