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15 results • Page
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12
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10 follow
Retrieve The Reads And Fastq From Bam File
samtools
updated 12 hours ago by
Reem
• 0 • written 11.0 years ago by
rehma.ar
▴ 290
2
votes
4
replies
289
views
Automate the Splitting of a VCF File by Sample (bcftools)
bcftools
vcf
updated 18 hours ago by
Pierre Lindenbaum
157k • written 2 days ago by
RogueBiochemist
• 0
2
votes
7
replies
663
views
Weirdness in annotation (missing allele frequencies)
allele-frequency
gnomad
annovar
updated 16 hours ago by
Jeremy Leipzig
21k • written 8 days ago by
Can Abdullah
• 0
2
votes
6
replies
260
views
Search RCSB with a list of protein names?
RCSB
protein
updated 2 hours ago by
Jiyao Wang
▴ 340 • written 1 day ago by
Joseph
• 0
0
votes
1
reply
102
views
How to import bigwig files into igvR
bigwig
igvr
updated 12 hours ago by
Trivas
★ 1.5k • written 15 hours ago by
ntsopoul
▴ 50
0
votes
1
reply
95
views
MAKER: WARNING: Could not get initialization lock. Trying Again...
gene
annotation
MAKER
prediction
updated 8 hours ago by
GenoMax
134k • written 15 hours ago by
memy
▴ 20
0
votes
1
reply
59
views
How to get ncol = nrow?
ncol
nrow
DESeq2
updated 2 hours ago by
Mark
★ 1.3k • written 4 hours ago by
Suha
• 0
0
votes
1
reply
57
views
vcf.gz to vcf
VCF
updated 2 hours ago by
Mark
★ 1.3k • written 4 hours ago by
sooni
▴ 10
0
votes
1
reply
76
views
bedtools intersect by position & stand not working even with common regions
bedtools
genomic
intersect
bedops
intervals
updated 2 hours ago by
rfran010
▴ 830 • written 8 hours ago by
Alewa
▴ 130
0
votes
3
replies
102
views
Encountering Error while Running 'make vcf' in Biostar Handbook
bugfix
biostarhandbook
vcf
53 minutes ago by
Tully
• 0
0
votes
1
reply
116
views
Unable to install HorvathMammalMethylChip40manifest packages
r
programming
updated 20 hours ago by
ATpoint
77k • written 22 hours ago by
Nibedita
• 0
0
votes
0
replies
6
views
DEG gene list and find common TF from public ChlP-Seq data
chip-seq
TF
10 minutes ago by
Joshua
• 0
0
votes
4
replies
306
views
Assessing Rockhopper's output
transcriptome
Rockhopper
RNA-seq
de-novo-assembly
18 hours ago by
langziv
▴ 50
0
votes
5
replies
192
views
Getting the overlap between two GTF files
file
RNA-seq
GTF
updated 18 hours ago by
GenoMax
134k • written 20 hours ago by
feather-W
• 0
0
votes
0
replies
72
views
TPM from STAR output without re-allign the file using RSEM or Salmon
bulkRNASEQ
STAR
RSEM
15 hours ago by
camillab.
▴ 140
15 results • Page
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Recent Votes
A: .gstmp extension on .bam files downloaded from google bucket; and EOF marker is
Comment: Significance testing of top vs. random SNPs
Answer: Search RCSB with a list of protein names?
A: running RAxML and MrBayes over concatinated multiple sequence alignments
Comment: Weirdness in annotation (missing allele frequencies)
Comment: Weirdness in annotation (missing allele frequencies)
Comment: ncbi error report log for validate fastq issue
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Comment: Getting the overlap between two GTF files
by
Alex Reynolds
35k
What would that be?
Answer: Encountering Error while Running 'make vcf' in Biostar Handbook
by
Tully
• 0
@ialbert ,I am deeply immersed in the fog and request the help ,please
Comment: bedtools intersect by position & stand not working even with common regions
by
rfran010
▴ 830
are you sure bedtools can handle the non-standard location of strand information?
Answer: Getting the overlap between two GTF files
by
rfran010
▴ 830
Maybe somebody knows something I don't, but I feel like bedtools should be able to handle your gtf files directly. If it's not done alre…
Answer: vcf.gz to vcf
by
Mark
★ 1.3k
As the error says, the file is not compressed. In linux the file extension is essentially optional. The file could be named `my.vcf.txt` ye…
Answer: Search RCSB with a list of protein names?
by
Jiyao Wang
▴ 340
You can use NCBI esearch to search the protein names against the structure database to get the PDB IDs, then retrieve the structures.
Answer: How to get ncol = nrow?
by
Mark
★ 1.3k
Without your actual data, it's hard to assist. I think what you're asking is 'how do I rename the rows of my dataframe(s)'. Taking the …
Comment: MAKER: WARNING: Could not get initialization lock. Trying Again...
by
GenoMax
134k
What kind of hardware are you running this on? You need to have the right kind of hardware (multiple CPU's not just cores), MPI libraries a…
Answer: Getting the overlap between two GTF files
by
Alex Reynolds
35k
Using `bedops --intersect` and `gtf2bed` will get their common genomic space: ``` bedops --intersect <(gtf2bed < transcripts.gtf) <(gtf2be…
Comment: Encountering Error while Running 'make vcf' in Biostar Handbook
by
Tully
• 0
```bash # Obtain the makefile curl -s http://data.biostarhandbook.com/make/snpcall.mk > Makefile # Run the makefile make vcf ``` Error me…
Comment: Encountering Error while Running 'make vcf' in Biostar Handbook
by
Tully
• 0
> System Information: Ubuntu 22.04 (WSL2) > > Shell: zsh > > Installation Verification: Yes, doctor.py OK [1]: https://www.biostarhand…
Comment: Retrieve The Reads And Fastq From Bam File
by
Reem
• 0
Did it affect the bamtofastq output file? if so how did you solve the problem? Thanks
Answer: How to import bigwig files into igvR
by
Trivas
★ 1.5k
You could try seeing if this fixes your issue with rtracklayer: https://support.bioconductor.org/p/p133244/
Comment: Weirdness in annotation (missing allele frequencies)
by
Jeremy Leipzig
21k
0.60625 is 97/160 so if you have 80 individuals in your VCF that's an internal allele frequency, not gnomAD
Comment: Weirdness in annotation (missing allele frequencies)
by
Can Abdullah
• 0
Yes, I was confused as well. I think the same. Maybe Annovar uses some other resources besides gnomad, but it does not make sense. Also, I …
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