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75 results • Page
2 of 2
Sort: replies
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Votes
Replies
0
votes
1
reply
152
views
Issue with merging in plink and eigensoft.
Eigensoft
Eigenstrat
Plink
updated 2 days ago by
bk11
★ 1.3k • written 2 days ago by
Jd
• 0
0
votes
1
reply
146
views
Quality Control of VCFs that used different genotyping arrays
bcftools
VCF
updated 1 day ago by
bk11
★ 1.3k • written 1 day ago by
Shane
• 0
1
vote
1
reply
133
views
Imputation server failing to see samples in VCF files
imputation
VCF
updated 1 day ago by
Ram
40k • written 1 day ago by
Ben
• 0
0
votes
1
reply
150
views
QC of genetic data
PLINK
updated 1 day ago by
bk11
★ 1.3k • written 1 day ago by
kl
▴ 10
0
votes
1
reply
158
views
Issues with featureCounts
featurecounts
rna-seq
differential-expression
updated 1 day ago by
Ram
40k • written 1 day ago by
Aime
• 0
0
votes
1
reply
117
views
Unable to install HorvathMammalMethylChip40manifest packages
r
programming
updated 20 hours ago by
ATpoint
77k • written 22 hours ago by
Nibedita
• 0
0
votes
1
reply
96
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
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
0
replies
97
views
How to obtain de pvalue of my DMRs using Bumphunter function from minfi
DMRs
3 days ago by
Irene
• 0
0
votes
0
replies
104
views
How to remove chimera from 16S Sanger contigs
sanger-sequencing
chimera
uchime
updated 4 days ago by
Ram
40k • written 4 days ago by
eimanpharmacist
▴ 20
0
votes
0
replies
122
views
How to annotate BED for tissue expression?
BED
annotation
5 days ago by
Fabio_bie88
• 0
0
votes
0
replies
85
views
TEtranscripts Tool in Galaxy
RNAseq
Transposable_Elements
TE_Transcripts
1 day ago by
gorizwango
▴ 30
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
0
replies
172
views
Current landscape of approaches to scRNA-seq with nanopore sequencers?
scRNA-seq
nanopore
single-cell
6 days ago by
LauferVA
3.7k
0
votes
0
replies
115
views
Spike-in normalization in ATAC-Seq with DiffBind
ATAC-Seq
spike-in
DiffBind
5 days ago by
frueher
• 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
0
votes
0
replies
113
views
filtering variants in a Strelka2 VCF file based on AD and AF
Filter
VCF
6 days ago by
Bogdan
★ 1.4k
0
votes
0
replies
122
views
Convert from limma voom normalized matrix each gene to high/low
limma-voom
RNA-SEQ
updated 2 days ago by
Ram
40k • written 2 days ago by
Manuel Sokolov Ravasqueira
▴ 100
0
votes
0
replies
127
views
Guide for ICD-10 to EFO conversion?
icd10
efo
2 days ago by
optimistsso4co3
▴ 100
0
votes
0
replies
110
views
Is the concept of a cofactor in an arcsinh transformation specific to Flow Cytometry?
FlowCytometry
flowCore
FlowVS
2 days ago by
gmiller
• 0
0
votes
0
replies
108
views
Can optimal cofactors for arcsinh transformation be calculated in parallel?
parallel
R
flowcytometry
flowCore
flowVS
2 days ago by
gmiller
• 0
0
votes
0
replies
83
views
rMats Run Does Not Generate More Than One Output Row Per File
Singularity
rMats
sif
1 day ago by
Y
• 0
0
votes
0
replies
129
views
Software for chimera detection of amplicon (e.g. 16S) nanopore reads
chimera
nanopore
amplicon
2 days ago by
rob_DNA
▴ 10
0
votes
0
replies
139
views
tensorQTL interaction issue
genomics
eqtl
genetics
qtl
3 days ago by
Solal
• 0
0
votes
0
replies
115
views
Select minimum set of SNPs from VCF file to identify a individual
selection
SNP
3 days ago by
Bioxbio
• 0
75 results • Page
2 of 2
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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Recent Replies
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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