Issues
- 2
Raw counts for downstream analysis
#24 opened by lubitelpospat - 7
nanocount for two condition
#15 opened by rezarahman12 - 1
Can I directly map reads directly to genes instead of transcripts to estimate the expression in gene level?
#37 opened by kerenzhou062 - 3
- 3
Nanocount vs Flair
#28 opened by sagnikbanerjee15 - 1
ERROR: No valid secondary alignments found in bam file. Were the reads aligned with minimap `-p 0 -N 10` options ?
#35 opened by lborcard - 1
- 1
Normalised the reads count
#33 opened by M-Chi-1 - 3
Est_count doesn't match records
#32 opened by KunFang93 - 2
- 2
- 1
- 0
Transcript expression level to Gene expression
#27 opened by vetmohit89 - 3
- 1
Too many reads are discarded
#26 opened by vetmohit89 - 1
How to deal with multiple ensemble IDs mapping to one gene symbol in a RNA-Seq dataset
#25 opened by vetmohit89 - 3
Adding option for cDNA reads
#12 opened by camillaugolini-iit - 2
Why NanoCount needs sorted alignments?
#20 opened by callumparr - 2
-N 100 hinder NanoCount accuracy?
#19 opened by callumparr - 1
alignmnet using sequin reference
#18 opened by rezarahman12 - 1
nanocount fast5 files
#17 opened by rezarahman12 - 1
about data of nanocount paper
#16 opened by rezarahman12 - 2
Different options when using minimap
#14 opened by Tomcxf - 1
Minimum number of ONT reads per sample
#13 opened by ms-gx - 2
Setting -3 to -1 to deactivate fails
#11 opened by josiegleeson - 1
No valid secondary alignment found in bam file
#10 opened by jhwan1203 - 5
Using with custom filtered alignments
#8 opened by josiegleeson - 6
ZeroDivisionError: division by zero
#5 opened by callumparr - 0
- 1
TPM values do not sum up to 1 million
#3 opened by lpryszcz - 0
Extract all references and length
#1 opened by a-slide - 2
Question about normalisation
#4 opened by tleonardi