Dear author,
I use CITE-seq-Count successfully got the results with mapping rate > 95%. But when I overlap cell barcode with my GEX gene expression data, there is no overlapping.
Even I convert barcode with "-1" suffix.
Here is my command:
CITE-seq-Count \
-R1 $indir/$r1 \
-R2 $indir/$r2 \
-t /project2/sli68423_1316/users/yang/u01/data/TAG_LIST.csv \
-cbf 1 -cbl 16 -umif 17 -umil 26 -cells 10000 --start-trim 10 \
-o citeseq_out_${tagname}
Here is the CITE-seq-Count output barcode:
zcat barcodes.tsv.gz | head
TCATGCCGTGCTACAT
GTCGTTCGTCAACGAG
AGATCGTCACCACACG
TGTTACTTCGCCTTCG
Here is the GEX data barcode:
zcat barcodes.tsv.gz | head
AAACCCAAGCCTCACG-1
AAACCCAAGCCTGACC-1
AAACCCAAGTATTGCC-1
AAACCCAAGTCGAATA-1
AAACCCACACGCTGCA-1
Do you have any suggestions to figure out the problem?
Thank you
Dear author,
I use CITE-seq-Count successfully got the results with mapping rate > 95%. But when I overlap cell barcode with my GEX gene expression data, there is no overlapping.
Even I convert barcode with "-1" suffix.
Here is my command:
Here is the CITE-seq-Count output barcode:
Here is the GEX data barcode:
Do you have any suggestions to figure out the problem?
Thank you