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758 results • Page
3 of 16
Sort: replies
Rank
Views
Votes
Replies
2
votes
6
replies
1.9k
views
How can you *consistently* download BioProject IDs from NCBI's BioSample database using Entrez Direct?
XML
ncbi
entrez-direct
updated 2 days ago by
Ram
43k • written 3.9 years ago by
millere
• 0
0
votes
6
replies
481
views
Differential Expression Analysis using DESeq2 in R
deseq2
R
updated 14 days ago by
swbarnes2
14k • written 14 days ago by
Erina
• 0
6
votes
6
replies
1.8k
views
agilent human all exon sureselct v7 bed file
exon
human
bed
v7
agilent
all
sureselect
updated 12 days ago by
MiladAD
▴ 10 • written 2.0 years ago by
soheil
• 0
10
votes
6
replies
10k
views
6 follow
CDS vs cDNA vs transcript for mapping RNA-Seq reads
Assembly
rna-seq
alignment
updated 21 days ago by
Antonio R. Franco
★ 5.1k • written 6.0 years ago by
williamsbrian5064
▴ 520
3
votes
6
replies
489
views
install package: package ‘gmwm’ is not available for this version of R
r
updated 5 days ago by
Pine
▴ 20 • written 12 days ago by
snajafy
• 0
0
votes
6
replies
218
views
ComplexHeatmap - How to change fontsize of rowAnnotation
ComplexHeatmap
3 hours ago by
hannes.bongartz
• 0
4
votes
6
replies
806
views
7 follow
Heatmap and rna-seq
RNA-Seq
Heatmap
updated 20 days ago by
dsull
★ 6.0k • written 24 days ago by
qudrat.nii
▴ 10
0
votes
6
replies
497
views
Use of Kraken output for functional analysis
metagenomics
kraken
shotgun
updated 23 days ago by
gv
• 0 • written 6 weeks ago by
Srinka
▴ 20
7
votes
6
replies
598
views
Filtering sam or bam file with maximum matching region
crisper-edited
alignment
match
26 days ago by
analyst
▴ 50
2
votes
6
replies
386
views
BWA alignment
Samtools
bam
updated 2 days ago by
a.alnawfal.1992
▴ 260 • written 4 days ago by
Vahid
• 0
0
votes
6
replies
2.1k
views
Copy number Variation analysis using conumee
R
software error
sequencing
genome
updated 8 days ago by
GenoMax
142k • written 3.2 years ago by
gs000095
▴ 10
3
votes
6
replies
2.0k
views
7 follow
DNA methylation preprocessing
SWAN
DNA
methylation
Funnorm
updated 21 days ago by
Ram
43k • written 2.4 years ago by
SYOSY
▴ 10
2
votes
5
replies
787
views
what's the genomic location and name of gene responsible for orange and black patches in calico cats
genomes
updated 27 days ago by
Jesse
▴ 770 • written 28 days ago by
Ann
★ 2.4k
2
votes
5
replies
954
views
Retrieval of Active site information programmatically
Catalytic
Python
Active
PDB
site
Site
updated 18 days ago by
Wayne
★ 2.0k • written 2.1 years ago by
arinjoy
• 0
0
votes
5
replies
6.0k
views
Calculate Radius of Gyration [python 3]
biopython
PDB
Radius of Gyration
python
protein
updated 27 days ago by
ndm1096
• 0 • written 6.5 years ago by
ac.research
▴ 30
2
votes
5
replies
10k
views
Find Corresponding Author: Doi Metadata?
updated 26 days ago by
Ram
43k • written 10.6 years ago by
Louis
▴ 150
0
votes
5
replies
329
views
A question about reference genome for creating the consensus sequence
fasta
fa
cram
genome
9 days ago by
me
• 0
1
vote
5
replies
493
views
How should I make kallisto indexes?
kallisto
updated 18 days ago by
dsull
★ 6.0k • written 4 weeks ago by
bioinfo
▴ 150
0
votes
5
replies
441
views
Is it possible to get a list of representative genomes from a past RefSeq release?
representative
ncbi
asembly
refseq
updated 22 days ago by
GenoMax
142k • written 23 days ago by
Bertalan_Takacs
▴ 90
2
votes
5
replies
409
views
Importing a fastq file
Fastq
updated 7 days ago by
size_t
▴ 120 • written 8 days ago by
oumo
• 0
3
votes
5
replies
342
views
Generating mpileup file using samtools
mpileup
samtools
updated 14 days ago by
Joe
21k • written 14 days ago by
Ruqaiya
• 0
0
votes
5
replies
428
views
Should I remove unlocalized scaffols in reference genome before alignment?
qualimap
alignment
minimap2
GRCh38
assembly
23 days ago by
njornet
▴ 20
1
vote
5
replies
271
views
Reconstruction of locus, order contigs
contigs
cluster
alignment
locus
updated 7 hours ago by
dthorbur
★ 2.0k • written 1 day ago by
BATMAN
• 0
0
votes
5
replies
279
views
Percentage coverage of reference genome by de novo genome
SAMtools
BWA
alignment
ddRAD
updated 9 days ago by
Joe
21k • written 9 days ago by
Lemonhope
• 0
2
votes
5
replies
540
views
Marking duplicates using UMIs
Deduplication
UMI
updated 25 days ago by
i.sudbery
19k • written 27 days ago by
Lipika
• 0
8
votes
5
replies
6.5k
views
ISCN annotation for SV/CN VCF files
SV
written 8 months ago by
a.beggs
▴ 60
3
votes
5
replies
397
views
Converting CRAM to FastQ
GATK
samtools
cram
SamToFastq
fastq
14 days ago by
Maverick
▴ 10
0
votes
5
replies
281
views
bbmerge (bbmap) ~ error with insert size file output
bbtools
bbmerge
bbmap
updated 2 days ago by
GenoMax
142k • written 2 days ago by
chrisk
• 0
3
votes
5
replies
352
views
Per base sequence content error in RNAseq analysis
RNA-seq
analysis
updated 25 days ago by
GenoMax
142k • written 25 days ago by
ahmad.sajad4541
• 0
1
vote
5
replies
372
views
Comparative Analysis of Algorithms for Implementing the FM-Index: Correctness, Complexity, and Use Cases
fmindex
bwt
updated 9 days ago by
Michael
54k • written 10 days ago by
qwertyuiop26
• 0
1
vote
5
replies
643
views
Cell barcode whitelists for DNBelab C Series High-throughput Single-cell RNA Series Library Preparation Set?
cell-barcode
MGI
DNBelab
single-cell
updated 24 days ago by
atowns21
• 0 • written 3 months ago by
benjamin.pyenson
• 0
3
votes
5
replies
638
views
SLURM submission problem: Indexing the Reference Genome is not done in STAR
align
RNA-Seq
linux
STAR
25 days ago by
n_navy
• 0
4
votes
5
replies
4.3k
views
Tool:
GRIDSS: the Genomic Rearrangement IDentification Software Suite
Assembly
Structural-Variation
Variant-Calling
updated 1 day ago by
dario.garvan
▴ 520 • written 7.2 years ago by
d-cameron
★ 2.9k
2
votes
5
replies
2.5k
views
identifying transgene insertion site in WGS
WGS
insertion site
trangene
de-novo
soap
updated 9 days ago by
Cameron.walker9900
• 0 • written 5.1 years ago by
Assa Yeroslaviz
★ 1.8k
2
votes
5
replies
425
views
How to trim transcripts using information from NCBI contamination screen report
RNAseq
assembly
transcriptome
contamination
21 days ago by
Lada
▴ 30
1
vote
5
replies
808
views
RNA seq differential expression analysis
RNA-seq
normalization
updated 28 days ago by
BioinfGuru
★ 1.7k • written 29 days ago by
rrehimi
• 0
5
votes
5
replies
341
views
Problem with data downloaded from Short Reads Archive (SRA)
SRA
DADA2
metabarcoding
updated 15 days ago by
atharvakarkare14
▴ 40 • written 15 days ago by
Begonia_pavonina
▴ 150
1
vote
5
replies
799
views
Converting IGV to Figure using Illustrator (or other tools)
Illustrator
IGV
written 6 months ago by
Daniel
▴ 30
0
votes
5
replies
434
views
6 follow
What purposes can TPM values be used for?
RNA-seq
TPM
Normalization
DESeq2
updated 14 days ago by
b.contreras.moreira
▴ 200 • written 15 days ago by
JH
• 0
2
votes
5
replies
540
views
Fetch table from clinvar database according to a list of rsid
python
clinvar
perl
19 days ago by
ashaneev07
▴ 20
5
votes
5
replies
666
views
Tutorial:
how to combine multiple RNAseq count files into a single dataframe in R and unix
Unix
RNAseq
R
updated 14 days ago by
Mbofire
• 0 • written 22 days ago by
Ming Tommy Tang
★ 3.9k
6
votes
5
replies
1.7k
views
How to calculate coverage of Nanopore long read data?
sequencing
coverage
2 days ago by
Arton
▴ 10
0
votes
5
replies
427
views
Telescope issue
Telescope
RNA-seq
updated 16 days ago by
GenoMax
142k • written 17 days ago by
eleven11
• 0
1
vote
5
replies
499
views
DYH17 Structure Prediction
BLAST
Protein-Structure-Prediction
24 days ago by
anasjamshed
▴ 120
1
vote
5
replies
351
views
install.packages("imudata") - package ‘imudata’ is not available for this version of R
r
updated 11 days ago by
Ram
43k • written 11 days ago by
snajafy
• 0
1
vote
5
replies
385
views
Introduce SNPs on FASTA
simulation
snps
haplotypes
pharmacogenetics
14 days ago by
Riccardo
▴ 10
1
vote
5
replies
249
views
Can I perform a correlation test with 3 biological replicates per condition?
RNA-Seq
deseq2
updated 1 day ago by
Ram
43k • written 1 day ago by
manuelmourato25
• 0
2
votes
5
replies
493
views
featureCounts output summary assigned value higher than uniquely mapped reads from HISAT2
RNA-seq
featureCounts
HISAT
updated 3 days ago by
Ram
43k • written 9 days ago by
Prawesh
• 0
2
votes
5
replies
645
views
MEGA Analysis Issue on High-Performance Computer
phylogenetic-analysis
MEGA
updated 27 days ago by
Mensur Dlakic
★ 27k • written 28 days ago by
Giorgio
• 0
1
vote
5
replies
215
views
Circos Plot to Visualize Chromatin Accessibility Changes from ATAC-seq Data
circos
atacseq
updated 2 days ago by
Pierre Lindenbaum
161k • written 2 days ago by
biology_inform
▴ 50
758 results • Page
3 of 16
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Recent Replies
Comment: How to handle duplicated genes in TCGA data?
by
Ngrin
• 0
Thanks @txema.heredia.The tool I am going to use only accepts gene symbols. This is the reason. So I cannot use ENS IDs.
Answer: Design for complex RNA-Seq experiment using Deseq2
by
swbarnes2
14k
This is a rather small experiment, I don't know that you can establish a meaningful baseline for each patient with a single pre sample, and…
Comment: GG Sankey plot
by
LauferVA
4.2k
@bk11 i changed this comment to an answer. if you disagree please let me know. thanks for sharing your knowledge. VAL
Comment: ComplexHeatmap - How to change fontsize of rowAnnotation
by
hannes.bongartz
• 0
Thanks for the input. Unfortunately, that didn't help either. I appreciate any other tips. Thank you
Answer: GG Sankey plot
by
bk11
★ 2.5k
You need to change your data table into a 'long' format. You can do something like this- GOs_childs_recursive <- GOs_childs_recursive …
Answer: Trimming tool
by
ntsopoul
▴ 60
I use Trim Galore which automatically recognizes adaptors. https://github.com/FelixKrueger/TrimGalore Here is the script I am using for…
Answer: Trimming tool
by
GenoMax
142k
There are plenty. `bbduk.sh` from BBMap suite (https://jgi.doe.gov/data-and-tools/software-tools/bbtools/bb-tools-user-guide/bbduk-guide/ )…
Comment: ComplexHeatmap - How to change fontsize of rowAnnotation
by
bk11
★ 2.5k
Please check out [in this link.][1] [1]: https://github.com/jokergoo/ComplexHeatmap/issues/349
Comment: Reconstruction of locus, order contigs
by
dthorbur
★ 2.0k
[Here](https://www.biostars.org/p/9544689/) is a forum post that may answer your question.
Comment: how to treat the replicates while performing WGCNA
by
andres.firrincieli
3.6k
> 1) I do not want to merge the MEs rather I asked about replicates, as > some replicates of same sample are showing different behavior for…
Comment: How to systematically check if a bam file is truncated
by
alanh
▴ 170
For more details about what `samtools quickcheck` actually checks for, add a few `-v`'s to the command line. $ samtools quickcheck -…
Comment: How to handle duplicated genes in TCGA data?
by
Zhenyu Zhang
★ 1.2k
Second what is said above, ensembl_id is the unique identifier. As a good bioinformatics habit, always use unique identifier for your anal…
Comment: ComplexHeatmap - How to change fontsize of rowAnnotation
by
hannes.bongartz
• 0
It doesn't work. The annotation labels are still in a default fontsize. I cant find a way to set the fontsize.
Comment: ComplexHeatmap - How to change fontsize of rowAnnotation
by
Ram
43k
Yes. The solution to most things with ComplexHeatmap is to play around with parameters.
Comment: Reconstruction of locus, order contigs
by
BATMAN
• 0
I do not want to re-annotate the genome. I ask if there is a way to extract the region aligned with the mauve, in .gbk format.
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