Latest
Open
Jobs
Tutorials
Tags
About
FAQ
Community
Planet
New Post
Log In
New Post
Latest
Open
News
Jobs
Tutorials
Forum
Tags
Planet
Users
Log In
Sign Up
About
Limit : this week
all time
today
this week
this month
this year
88 results • Page
1 of 2
Sort: Rank
Rank
Views
Votes
Replies
0
votes
0
replies
32
views
My rMATS output file is not showing gene symbols and only XLOC gene ID are being shown.
rMATS
rMATS-turbo
2 hours ago by
Nipan
• 0
1
vote
3
replies
75
views
Using STAR aligner to build index of hg38
hg38
STAR
alignment
RNAseq
index
updated 1 hour ago by
GenoMax
134k • written 3 hours ago by
Grace
• 0
0
votes
0
replies
63
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
71
views
Hugo_Symbol to Entrez ID
hugo
bioinformatics
entrez
ids
symbols
just now by
shakyaram079
• 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 4 hours ago by
Mensur Dlakic
★ 24k • written 17 hours ago by
Mohd
▴ 40
0
votes
1
reply
105
views
Understanding TCGA barcodes with dot in the fieldname
tcga
updated 19 hours ago by
Ram
40k • written 20 hours ago by
Tahsin
• 0
0
votes
0
replies
78
views
Compare peaks between clusters in sc-ATAC
Peak-Calling
Epigenome
scATAC-seq
updated 19 hours ago by
Ram
40k • written 20 hours ago by
Ahmed.waraky
▴ 10
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
3
replies
180
views
Weirdness in annotation (missing allele frequencies)
allele-frequency
gnomad
annovar
updated 1 day ago by
Ram
40k • written 1 day ago by
Can Abdullah
• 0
1
vote
3
replies
137
views
Finding sequences in unannotated genomes using reference coordinates
consensus
VCF
updated 1 day ago by
Ram
40k • written 1 day ago by
Prangan
▴ 20
0
votes
1
reply
133
views
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
0
replies
89
views
Why dbConnect GEOmetadb_demo.sqlite shows some information while dbConnect GEOmetadb.sqlite shows no information
R
GEO
GEOmetadb
updated 1 day ago by
Pierre Lindenbaum
157k • written 1 day ago by
nonaddldy
▴ 10
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
99
views
Gene enrichment analysis of prokaryotes gene
prokaryotes
GO
enrichment
DEG
1 day ago by
Genta
• 0
0
votes
0
replies
109
views
High pvalues when using clusterProfiler for seurat
clusterProfiler
1 day ago by
Ahmed
• 0
5
votes
7
replies
314
views
Salmon index not progressing
salmon
updated 23 hours ago by
Michael
53k • written 1 day ago by
camillab.
▴ 130
0
votes
0
replies
105
views
scanpy problem for empty cells
scanpy
updated 1 day ago by
Ram
40k • written 1 day ago by
Andy
▴ 90
0
votes
0
replies
110
views
Current landscape of approaches to scRNA-seq with nanopore sequencers?
scRNA-seq
nanopore
single-cell
updated 1 day ago by
Ram
40k • written 1 day ago by
LauferVA
3.7k
0
votes
1
reply
141
views
How to download genomes and proteins from JGI in bulk via the command line?
jgi
cli
updated 1 day ago by
Ram
40k • written 1 day ago by
O.rka
▴ 680
0
votes
1
reply
143
views
OMA in AWS cloud
OMA
AWS
updated 1 day ago by
Ram
40k • written 2 days ago by
Ksel
• 0
0
votes
6
replies
281
views
genome data downloads for various strains
gisaid
hass-marr
updated 1 day ago by
Ram
40k • written 2 days ago by
iftikharmaryam123
• 0
0
votes
0
replies
131
views
Illumina methylation EPIC V2 array
ewas
methylation
enrichment
missMethyl
EPIC
2 days ago by
juliviglino
• 0
0
votes
1
reply
177
views
Esearch, Epost, and Efetch for Large Datasets in Biopython
eutils
biopython
entrez
updated 2 days ago by
Ram
40k • written 2 days ago by
Salem
• 0
3
votes
10
replies
434
views
STAR index not working
STAR
RNA-Seq
1 day ago by
camillab.
▴ 130
2
votes
3
replies
260
views
Can I infer the fraction of replicating cells from bulk RNA-seq data?
replication
apoptosis
updated 3 days ago by
Ram
40k • written 3 days ago by
txema.heredia
▴ 80
0
votes
1
reply
149
views
Prank checkpoint and restore?
prank
alignment
updated 3 days ago by
Ram
40k • written 3 days ago by
Pit
• 0
0
votes
13
replies
469
views
STAR Intron Motif Script Gives Segmentation fault Error
STAR
Linux
2 hours ago by
Y
• 0
1
vote
3
replies
216
views
Sub-sampleing bam files based on sequencing_summary.txt (guppy output)
samtools
guppy
updated 3 days ago by
GenoMax
134k • written 3 days ago by
anika.john
• 0
0
votes
0
replies
104
views
Any way to predict hormone biosynthesis pathways in understudied organisms?
genomics
orthologs
biosynthesis-pathway
updated 3 days ago by
Ram
40k • written 3 days ago by
Mark
• 0
2
votes
4
replies
288
views
Refseq annotation | Populus trichocarpa
R
RNA-seq
plants
Refseq
updated 3 days ago by
Ram
40k • written 3 days ago by
P
• 0
1
vote
1
reply
177
views
Read Counts from BAM file
bam
samtools
qualimap
readcount
updated 3 days ago by
ATpoint
76k • written 3 days ago by
Smriti
• 0
0
votes
2
replies
217
views
Is it okay to just average the log2FC values across different cell types in pseudobulk scRNA-seq data?
scrna-seq
rna-seq
log2fc
3 days ago by
JLee
• 0
0
votes
1
reply
168
views
Identify parent of each read in a GAF
gaf
vgteam
vg
updated 3 days ago by
Jordan M Eizenga
▴ 360 • written 4 days ago by
cfourps
▴ 10
0
votes
3
replies
225
views
Errors while trying to run Scenic
Scenic
updated 3 days ago by
GenoMax
134k • written 4 days ago by
Stavroula
• 0
0
votes
3
replies
241
views
How to find target genes From RNA seq data?
Cotton
DGE
RNA-seq
updated 4 days ago by
Ram
40k • written 4 days ago by
Fizzah
▴ 30
0
votes
0
replies
121
views
maftools - median survival time doesn't match plot
R
survival
maftools
K-M
4 days ago by
BioGuy
• 0
0
votes
1
reply
152
views
vg rna pantranscriptome
rna
vg
updated 4 days ago by
Jordan M Eizenga
▴ 360 • written 4 days ago by
z
• 0
0
votes
0
replies
112
views
Genetic distance in cM from VCF of non-reference species to run Beagle
plink
beagle
vcf
updated 4 days ago by
Ram
40k • written 4 days ago by
AndrMod
• 0
1
vote
4
replies
266
views
rRNA filtering from human RNA-seq data
rRNA
RNA-seq
4 days ago by
deniz
▴ 10
0
votes
5
replies
321
views
manhattan plot with vcf information
R
manhattan
vcf
updated 2 days ago by
dthorbur
▴ 550 • written 4 days ago by
sooni
▴ 10
0
votes
0
replies
423
views
after gatk VariantAnnotator -V *_com_norm.vcf -A AlleleFraction -O *_norm_AB.vcf There "nan,nan" or "nan" in my vcf file
gatk
AlleleFraction
VariantAnnotator
updated 4 days ago by
Ram
40k • written 4 days ago by
zhuo
• 0
2
votes
0
replies
132
views
the dispersion estimation of edgeR and DESeq2
estimation
dipersion
edgeR
DESeq2
4 days ago by
tommy
▴ 30
2
votes
3
replies
268
views
Genewise output help
genewise
updated 4 days ago by
Jean-Karim Heriche
26k • written 4 days ago by
lorenzoedg
• 0
2
votes
1
reply
162
views
Best Tools and Practices for CNV Variant Calling in WES Data
CNV
WES
updated 5 days ago by
Pierre Lindenbaum
157k • written 5 days ago by
Nadav
▴ 10
0
votes
2
replies
180
views
Identify genes for mapped reads with combined human-7HPV genome index
star
samtools
updated 5 days ago by
Ram
40k • written 5 days ago by
r.j.lock
• 0
0
votes
0
replies
117
views
Data for pathview() (KEGG Pathway Map) after EdgeR
EdgeR
LogFC
pathview
KEGG
5 days ago by
Ann
▴ 10
0
votes
0
replies
263
views
GTF/Reference genome adjustments? Gene-based differential expression analysis of genetically modified mouse line
RNA-seq
DGE
updated 5 days ago by
Ram
40k • written 5 days ago by
alex
• 0
0
votes
0
replies
136
views
Selecting SNPs for two-sample Mendelian randomization study/analysis
Two-sample
SNPs
Mendelian
randomization
5 days ago by
huynguyenacademia
• 0
0
votes
0
replies
128
views
cosine simialrity of mutation signature analysis
similarity
Mutational
analysis
signature
cosine
5 days ago by
probioquestioner
• 0
0
votes
1
reply
203
views
Significance testing of top vs. random SNPs
SNPs
significance
variance
statistical
updated 2 days ago by
dthorbur
▴ 550 • written 5 days ago by
am29
▴ 30
88 results • Page
1 of 2
Recent Votes
Comment: Error: cannot open file 2 for reading From Cufflinks Version 2.2.1 When Attempti
Comment: Error in bowtie2
Recommended Tools For Alternative Splicing Detection From Rna-Seq Data
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.
Recent Locations •
All
Canada,
just now
Denmark,
1 minute ago
Cambridge, MA,
4 minutes ago
Canada,
4 minutes ago
University of Utah,
6 minutes ago
United States,
9 minutes ago
United States,
11 minutes ago
Recent Awards •
All
Popular Question
to
langziv
▴ 50
Popular Question
to
Emily
▴ 30
Popular Question
to
Bogdan
★ 1.4k
Popular Question
to
paria
▴ 70
Popular Question
to
Ahmed.waraky
▴ 10
Teacher
to
fracarb8
★ 1.2k
Scholar
to
antonioggsousa
2.8k
Recent Replies
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
Comment: Deepvariant variant calling by singularity
by
jeffhsu3
• 0
I am having a similar issue was this ever resolved? Getting this error: I0922 22:22:08.794076 140356687390528 make_examples_core.py:257] O…
Traffic: 2213 users visited in the last hour
Content
Search
Users
Tags
Badges
Help
About
FAQ
Access
RSS
API
Stats
Use of this site constitutes acceptance of our
User Agreement and Privacy Policy
.
Powered by the
version 2.3.6