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213 results • Page
5 of 5
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133
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High amount of intronic/intergenic reads in SMARTer stranded total bulk RNAseq
RNA-seq
DNA
SMARTer
updated 1 day ago by
Ram
40k • written 1 day ago by
Mat
▴ 60
0
votes
3
replies
197
views
ATAC-seq troubleshoot - Just Noise
ATAC-seq
updated 1 day ago by
Ram
40k • written 1 day ago by
vk
▴ 40
0
votes
0
replies
175
views
What metrics to use to calculate variant library evenness or uniformity or bias
library-bias
variant
updated 6 days ago by
Ram
40k • written 7 days ago by
eli_bayat
▴ 90
0
votes
0
replies
75
views
bedGraph for Coverage of Insert from Paired-End Data?
genome
awk
coverage
bed
paired-end
22 hours ago by
vanbelj
▴ 40
0
votes
1
reply
105
views
Understanding TCGA barcodes with dot in the fieldname
tcga
updated 20 hours ago by
Ram
40k • written 21 hours ago by
Tahsin
• 0
0
votes
0
replies
78
views
Compare peaks between clusters in sc-ATAC
Peak-Calling
Epigenome
scATAC-seq
updated 20 hours ago by
Ram
40k • written 21 hours ago by
Ahmed.waraky
▴ 10
0
votes
1
reply
194
views
How to create structural variants ground truth for alignment of two long-read genome assemblies?
yeast
assembly
structural-variation
SV-callers
updated 11 hours ago by
Christophe
• 0 • written 3 days ago by
Thomas
• 0
0
votes
1
reply
129
views
Modify the code to take most abundant reads from a cluster and process it.
cd-hit-est
clustering
updated 5 hours ago by
Mensur Dlakic
★ 24k • written 17 hours ago by
Mohd
▴ 40
0
votes
6
replies
301
views
Highly inflated p-values in GWAS by regenie
regenie
plink
gwas
updated 4 hours ago by
4galaxy77
2.8k • written 1 day ago by
cwwong13
▴ 20
0
votes
0
replies
35
views
My rMATS output file is not showing gene symbols and only XLOC gene ID are being shown.
rMATS
rMATS-turbo
3 hours ago by
Nipan
• 0
0
votes
13
replies
474
views
STAR Intron Motif Script Gives Segmentation fault Error
STAR
Linux
2 hours ago by
Y
• 0
0
votes
0
replies
64
views
Convert RNASeq V2 data in cBioPortal having RSEM normalized results to TPM values
bioinformatics
TPM
RNASeqV2
cbioportal
RSEM
updated 2 hours ago by
4galaxy77
2.8k • written 11 hours ago by
shakyaram079
• 0
0
votes
2
replies
75
views
Hugo_Symbol to Entrez ID
hugo
bioinformatics
entrez
ids
symbols
21 minutes ago by
shakyaram079
• 0
213 results • Page
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Comment: Error: cannot open file 2 for reading From Cufflinks Version 2.2.1 When Attempti
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Comment: Using STAR aligner to build index of hg38
Answer: How to sort using samtools
The Biostar Handbook. A bioinformatics e-book for beginners.
The Biostar Handbook. A bioinformatics e-book for beginners.
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Comment: Hugo_Symbol to Entrez ID
by
shakyaram079
• 0
Yes sure. These are all gene IDs BZRAP1, C19orf60, TCEB3 and so on.
Comment: Error: cannot open file 2 for reading From Cufflinks Version 2.2.1 When Attempti
by
Y
• 0
I tried the commands you recommended in the bash/command line. When I tried `find "${bam_directory}" -type f -name "*.bam" | xargs samtools…
Comment: Hugo_Symbol to Entrez ID
by
GenoMax
134k
Can you provide some examples of HUGO ID's you are unable to convert?
Comment: Using STAR aligner to build index of hg38
by
GenoMax
134k
GTF file includes gene models/annotation information. You could also use a program like `salmon/kallisto` with just human transcriptome to…
Comment: Error: cannot open file 2 for reading From Cufflinks Version 2.2.1 When Attempti
by
Pierre Lindenbaum
157k
then test each files. find "${bam_directory}" -type f -name "*.bam" | xargs samtools quickcheck file "${reference_gen…
Answer: Ties in reranked list
by
alserg
▴ 840
The problem here is not the ties, but that your gene IDs in the pathway list (ensemble human genes) does not match the names of the stats v…
Comment: Error: cannot open file 2 for reading From Cufflinks Version 2.2.1 When Attempti
by
Y
• 0
I did not use the space between the `-u` flag and the `-o` flag (the blank line) but I did do what you recommended: # Run CuffDiff wit…
Answer: Error: cannot open file 2 for reading From Cufflinks Version 2.2.1 When Attempti
by
Pierre Lindenbaum
157k
how about simply trying: ``` cuffdiff -u "${annotation_gtf}" \ -o "${output_directory}" \ -b "${reference_genome}" \ -p "${num_th…
Comment: Using STAR aligner to build index of hg38
by
Grace
• 0
Yes, I know also need a GTF file. So the GTF file will include RNA information? Thanks for your answer!!
Comment: STAR Intron Motif Script Gives Segmentation fault Error
by
Y
• 0
I will try and figure it out on my own given what you all have mentioned. Thank you for your time.
Comment: Using STAR aligner to build index of hg38
by
Amitm
★ 2.2k
Have you gone through the manual [here][1]. In addition to the genome fasta file, you would also need a GTF file (of gene annotations) to b…
Comment: Highly inflated p-values in GWAS by regenie
by
4galaxy77
2.8k
You still definitely need to include principle components as covariates, even if your data is from the same ethnicity. Not including those …
Answer: How to create structural variants ground truth for alignment of two long-read ge
by
Christophe
• 0
Hi, D-genies is using minimap2 to align both genomes and minimap2 is chaining local alignments to produce a global one. If the SV are sm…
Comment: Ties in reranked list
by
Hamza
• 0
In this case there are no results in my fgsea object unfortunately
Comment: Genes with promoter and enhancer regions as GTF
by
abis.1819104
• 0
how to generate promoters.bed and enhancer.bed files from gtf file
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