Issues
- 3
- 4
In a given SNP region, what are the criteria being used to categorize a cell as WT(0/0), heterozygote(1/0), and homozygote(1/1)?
#109 opened by jiehuichen - 5
UMI Collapsing
#121 opened by grasshoffm - 0
Matching SNPs to cell barcode
#124 opened by malonzm1 - 7
Unable to install through anaconda
#120 opened by Angelos-Gk - 2
Combined max depth is above 1M. Potential memory hog! / Recommendations for maxDepth?
#122 opened by bbimber - 2
[E::bgzf_flush] File write failed (wrong size)
#117 opened by ghuls - 3
Could not retrieve index file for .bam
#119 opened by nansne - 6
runtime and expected output
#78 opened by ahoffrichter - 1
Strand specificity
#118 opened by flde - 0
- 3
The 19 of 20 parallelized workers always strike far before the whole job is done
#88 opened by mimi3421 - 1
- 1
Is there a good way to identify and add the gene names to the output vcfs?
#113 opened by pchatterjee7 - 1
Use cellSNP on a big BAM file
#111 opened by RosaDeSa - 2
minimal minor allele count filter?
#108 opened by chilampoon - 4
- 2
cellsnp-lite on data from 1 donor
#106 opened by astaburuaga-garcia - 2
get unwanted allele in ALT column
#105 opened by jiehuichen - 5
- 6
- 5
OTH ratio 1
#93 opened by flde - 6
- 0
- 1
postprocessing cellsnp outputs
#96 opened by maxozo - 4
miscount alleles single-cell ATAC-seq
#95 opened by raul-w - 5
- 5
Question for minMAF parameter
#77 opened by fe4960 - 8
Filter SNPs by minMAF after running cellsnp-lite
#90 opened by flde - 3
Application to Slide-seq V2 returns empty vcf
#91 opened by kzb193 - 1
How to use cellsnp-lite
#89 opened by DaliBAmor - 2
Handling haploid cells
#87 opened by haigdjambazian - 4
more reads filter options?
#85 opened by zhentaoyoung - 5
Genotyping ATAC from WES vcf
#86 opened by ollieeknight - 2
hg38 chromsome names in 1000G VCF and 10X BAM
#84 opened by jnktsj - 2
Duplicate barcodes error?
#80 opened by terencewtli - 3
Barcodes File Clarification
#81 opened by DarioS - 2
AF for candidate SNP
#66 opened by Zepeng-Mu - 2
- 2
Automatically detect all chromosomes in bam
#76 opened by chilampoon - 1
- 1
Unable to install CellSNP-Lite from conda
#74 opened by aseyedia - 1
Had any scripts to pick the distinctive SNP site from vireo file GT_donors.vireo.vcf.gz gene to distinguish multiple sample using PCR experiment
#73 opened by honghh2018 - 1
how can i build the preprocess vcf for mouse, like human common SNP vcf file, using GATK google warehouse snp data
#72 opened by honghh2018 - 2
- 1
Huge 10X scRNA-seq mouse data
#70 opened by alexfernandes8a - 1
- 0
The mutation matrix input for SCITE
#69 opened by alanfoleynibrt - 1
How to set -p (Slurm)
#67 opened by flde - 5