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1
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397
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Which type of variant caller should I use in a WES normal cell line sample?
variant-caller
WES
updated 10 months ago by
ATpoint
81k • written 10 months ago by
bompipi95
▴ 150
0
votes
0
replies
498
views
Picard's CollectGcBiasMetrics gc-bias plot- help with interpretation
picard
gc-bias
wes
11 months ago by
bompipi95
▴ 150
1
vote
3
replies
1.2k
views
Off-target % for whole-exome sequencing panel
WES
updated 11 months ago by
trausch
★ 1.9k • written 11 months ago by
bompipi95
▴ 150
0
votes
1
reply
520
views
WES variant calling with DNBSEQ-T7 - technical quality assessment
WES
DNA-seq
GATK
variant-calling
mutect2
updated 11 months ago by
colindaven
6.3k • written 11 months ago by
bompipi95
▴ 150
0
votes
2
replies
583
views
Integrating single-nucleus RNA-seq and single-cell RNA-seq datasets
snRNAseq
single-cell
scRNAseq
13 months ago by
bompipi95
▴ 150
1
vote
2
replies
912
views
Check my understanding - difference between number of reads sequenced and Seurat nCount_RNA
scRNAseq
13 months ago by
bompipi95
▴ 150
6
votes
3
replies
806
views
To batch correct or analyse separately?
scRNA-seq
batch
correction
14 months ago by
bompipi95
▴ 150
4
votes
4
replies
825
views
Aligning reads from mouse samples that express 1 human gene
realignment
updated 17 months ago by
swbarnes2
14k • written 17 months ago by
bompipi95
▴ 150
2
votes
1
reply
721
views
t2t human reference genome for RNA-seq
t2t
hs1
RNA-seq
updated 13 months ago by
O.rka
▴ 710 • written 17 months ago by
bompipi95
▴ 150
6
votes
2
replies
881
views
Identifying tumor vs normal cells in scRNAseq samples
seurat
CNV
scRNA-seq
cancer
updated 19 months ago by
benformatics
3.9k • written 19 months ago by
bompipi95
▴ 150
2
votes
2
replies
1.1k
views
Help with kallisto-bustools: how to interpret the inspect.json output file
scRNAseq
bustools
kallisto
updated 10 months ago by
Ram
43k • written 23 months ago by
bompipi95
▴ 150
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