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88 results • Page
1 of 2
Sort: replies
Rank
Views
Votes
Replies
0
votes
13
replies
472
views
STAR Intron Motif Script Gives Segmentation fault Error
STAR
Linux
2 hours ago by
Y
• 0
0
votes
11
replies
691
views
Normalization for microarrays >1000+ samples?
microarray
normalization
oligo
3 days ago by
evmae
• 0
1
vote
10
replies
875
views
Deepvariant variant calling by singularity
deepvariant
singularity
conda
docker
updated 12 hours ago by
jeffhsu3
• 0 • written 11 weeks ago by
fra.silvestro99
▴ 10
3
votes
10
replies
434
views
STAR index not working
STAR
RNA-Seq
1 day ago by
camillab.
▴ 130
0
votes
8
replies
734
views
Chipseq analysis on repeat genes
galaxy
repeatmasker
ChIP-seq
repeat-elements
ATAC-seq
1 day ago by
pb11
▴ 10
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
7
replies
779
views
Mugsy error -directory must be a directory
Mugsy
updated 2 days ago by
Ram
40k • written 2.8 years ago by
A_heath
▴ 140
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
6
replies
842
views
FACS (Fluorescence-activated cell sorting NOT cyTOF),Automating the removal of dead and duplicated cells
FACS
2 days ago by
ccbb7aab4
▴ 20
1
vote
5
replies
474
views
Idat raw data conversion
idat
updated 5 days ago by
Giulio Genovese
▴ 330 • written 7 days ago by
Zi
• 0
8
votes
5
replies
1.6k
views
BLASTp command line : filtering results by a minimum % of identity and % coverage
BLASTp
updated 2 days ago by
Ram
40k • written 23 months ago by
A_heath
▴ 140
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
4
votes
5
replies
467
views
Pre-processing for single cell RNAseq: Hard thresholds, data (cluster)-driven or both?
scRNA-seq
5 days ago by
psm
▴ 100
1
vote
5
replies
664
views
Mugsy percentage of identity
Mugsy
Genome-alignment
updated 2 days ago by
Ram
40k • written 2.5 years ago by
A_heath
▴ 140
2
votes
4
replies
414
views
Help with celltype annotation
seurat
single-cell
6 days ago by
Chris
▴ 180
3
votes
4
replies
341
views
Weighted analysis
RNA-seq
4 days ago by
Peter
• 0
1
vote
4
replies
266
views
rRNA filtering from human RNA-seq data
rRNA
RNA-seq
4 days ago by
deniz
▴ 10
3
votes
4
replies
411
views
During alignment STAR has stopped at started alignment step
STAR
updated 3 days ago by
Ram
40k • written 6 weeks ago by
Santhi
• 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
0
votes
3
replies
724
views
How to add translation of CDS in Artemis?
translation
Artemis
updated 2 days ago by
Ram
40k • written 2.7 years ago by
A_heath
▴ 140
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
3
replies
2.0k
views
extraction of original gene iDs from reference annotation file
rna-seq
updated 3 days ago by
aishwarya
• 0 • written 5.2 years ago by
blooming.daisy333
▴ 110
2
votes
3
replies
1.5k
views
Racon command line with paired-ends Illumina reads
Illumina
Racon
updated 2 days ago by
Ram
40k • written 2.0 years ago by
A_heath
▴ 140
1
vote
3
replies
340
views
What is "intersectional genetic strategy"? How does it work? What can it do?
cell-subtypes
6 days ago by
Ethan Lee
• 0
0
votes
3
replies
327
views
RSubread DESeq2
RNA-seq
subread
differential-expression
deseq2
updated 5 days ago by
Ram
40k • written 14 days ago by
Beyza
• 0
1
vote
3
replies
667
views
How to determine plasmid or chromosomal origin?
plasmid
chromosomal-origin
updated 2 days ago by
Ram
40k • written 3.0 years ago by
A_heath
▴ 140
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
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
1
vote
3
replies
217
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
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
3
replies
225
views
Errors while trying to run Scenic
Scenic
updated 4 days ago by
GenoMax
134k • written 4 days ago by
Stavroula
• 0
1
vote
3
replies
259
views
Question regarding MACS2 approach of peak calling
MACS2
sequencing-depth
chipseq
updated 3 days ago by
ATpoint
76k • written 12 days ago by
rkc5
• 0
0
votes
3
replies
261
views
Extracting/assembling organellar reads from RNAseq data
transcriptome
star
alignment
mapping
updated 5 days ago by
LChart
3.3k • written 12 days ago by
Miles
• 0
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
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
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
0
votes
3
replies
296
views
RdRp scan - identifying/detecting viruses- metagenomic workflow- need help
RdRp
virus-detection
metagenomic
updated 5 days ago by
Ram
40k • written 9 days ago by
eric--carron
• 0
2
votes
2
replies
253
views
Pangenome using Orthofinder
OrthoFinder
Pangenome
bacteria
5 days ago by
kirankumareripogu
▴ 10
1
vote
2
replies
270
views
functional analysis prediction
functionalanalysis
metabarcoding
16S
5 days ago by
safeassli
• 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
1
vote
2
replies
255
views
Multiple testing adjustment for stepwise model selection
statistics
5 days ago by
mel22
▴ 100
3
votes
2
replies
405
views
Recommended way to normalize SmartSeq2 gene expression matrix to better match 10X expression data
rna-seq
smartseq2
r
updated 3 days ago by
yhdist
▴ 70 • written 5 days ago by
Cookin
• 0
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
2
replies
71
views
Hugo_Symbol to Entrez ID
hugo
bioinformatics
entrez
ids
symbols
just now by
shakyaram079
• 0
2
votes
2
replies
202
views
Clustering algorithm based on grouping sequences into gene families
gene-families
clustering
updated 5 days ago by
Ram
40k • written 6 days ago by
francesco
• 0
0
votes
1
reply
376
views
Close genome comparison
Mauve
Mugsy
genome-comparison
GSAlign
updated 2 days ago by
Ram
40k • written 19 months ago by
A_heath
▴ 140
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
0
votes
1
reply
754
views
How to identify specific region using Mauve?
Mauve
primers
updated 2 days ago by
Ram
40k • written 2.8 years ago by
A_heath
▴ 140
0
votes
1
reply
898
views
Issue interpreting plasmidSPAdes output
plasmidSPAdes
updated 2 days ago by
Ram
40k • written 2.9 years ago by
A_heath
▴ 140
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
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.
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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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