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119 results • Page
2 of 3
Sort: Rank
Rank
Views
Votes
Replies
0
votes
1
reply
168
views
Co-Expression of All Genes with a Single Gene (Spatial Transcriptomics)
Transcriptomics
Correlation
Seurat
scRNA-seq
Spatial-Transcriptomics
updated 4 days ago by
jv
★ 1.2k • written 5 days ago by
ivingan
• 0
0
votes
1
reply
184
views
How to find complete overlaps between between multiple .bed files with bedtools
bedtools
granges
updated 5 days ago by
Pierre Lindenbaum
154k • written 5 days ago by
Alewa
▴ 110
0
votes
2
replies
194
views
Don't see uploaded files for linking in EGA (European Genome Archive)
EGA
5 days ago by
optimistsso4co3
▴ 100
0
votes
0
replies
115
views
Tools for network enrichment analysis in bacteria
network-enrichment-analysis
5 days ago by
langziv
▴ 20
1
vote
2
replies
2.0k
views
Error in Adding 1000Genomes Ancestral Allele info: Using VCF tools fill-aa
vcftools
samtools
faidx
tabix
1000Genomes
updated 5 days ago by
barslmn
★ 1.5k • written 5.6 years ago by
shrutishreyajha
▴ 10
1
vote
3
replies
329
views
Variant calling analysis
vcf
variant-calling
wgs
updated 5 days ago by
Medhat
9.6k • written 6 days ago by
namck
• 0
0
votes
0
replies
161
views
Comparing gene expression with copy number variation in TCGA
BiomaRt
TCGABiolinks
6 days ago by
Will Yam
▴ 30
0
votes
1
reply
250
views
Trimmomatic run error
Trimmomatic
adap
updated 6 days ago by
Pierre Lindenbaum
154k • written 7 days ago by
eshrakaali_p
• 0
1
vote
5
replies
491
views
kraken on nt library
kraken
nt
4 days ago by
Francois Piumi
▴ 30
3
votes
1
reply
253
views
chromosome location to gene name and aa change
variant-annotation
6 days ago by
Zi
• 0
0
votes
2
replies
347
views
modelling time series data from different individuals
modeling
3 days ago by
Sara
▴ 220
0
votes
1
reply
322
views
Reducing the size of raw sequencing data in fastq format by using a simplified quality score
fastq
compression
updated 6 days ago by
ATpoint
72k • written 8 days ago by
rls_08
▴ 40
1
vote
3
replies
346
views
how to do an "reverse" oncoplot in maftools
maftools
Rstudio
updated 4 days ago by
Ram
39k • written 8 days ago by
JULIA HELENA
• 0
0
votes
0
replies
186
views
Error in running Abyss assembler for chicken genome assembly
abyss
assembly
genome
fasta
1 day ago by
Maliha
▴ 20
4
votes
6
replies
509
views
How to pass from DNA to AA fasta
genetics
updated 5 days ago by
Buffo
★ 2.2k • written 8 days ago by
Anderson Stiward
• 0
2
votes
6
replies
516
views
how to make a venn plot with data frame in R
plot
R
Venn
6 days ago by
satva72
• 0
7
votes
12
replies
812
views
Integrated genes from bulk RNA seq and ATAC seq
bulk-RNA
integrated
ATAC-seq
updated 3 days ago by
Sasha
▴ 180 • written 9 days ago by
Chris
▴ 100
4
votes
8
replies
502
views
Error while running nf-core/rnaseq pipeline
nf-core
RNA-seq
4 days ago by
eesha28112001
• 0
2
votes
6
replies
359
views
Find data-based Gene_IDs for unknown gene_IDs in gtf.file
RNA-SEQ
annotation
GO-term
6 days ago by
Pegasus
▴ 90
0
votes
4
replies
298
views
desgin a primer for CDS
gene
pcr
14 hours ago by
yuxiang
• 0
1
vote
3
replies
322
views
Retrieve Promoter Sequences by GeneID
GeneID
by
Sequences
Retrieve
Promoter
updated 4 days ago by
lieven.sterck
14k • written 4 weeks ago by
alessandro.alma00
• 0
0
votes
4
replies
483
views
From VCF to BEAGLE format with multiple chromosomes
vcf
vcftools
beagle
gvcf
3 days ago by
Begonia_pavonina
▴ 100
0
votes
3
replies
447
views
how to calcul risk score with a prognostic genes
riskscore
multivariate
analysis
prognostic
model
updated 22 hours ago by
Maryam
• 0 • written 7 months ago by
Nobody
▴ 30
0
votes
4
replies
468
views
BBduk reading fastq from S3 directly - Is it possibile?
BBduk
BBTools
BBMap
6 days ago by
Marko
▴ 10
0
votes
0
replies
594
views
Htslib c++ library faidx fetch region
samtools
cpp
faidx
htslib
updated 5 days ago by
Ram
39k • written 2.6 years ago by
rah
▴ 20
0
votes
2
replies
802
views
How to get a list of aligned read and reference positions using samtools
samtools
api
htslib
Cpp
c
updated 5 days ago by
Ram
39k • written 3.1 years ago by
Aref.Ariyapour
• 0
0
votes
4
replies
1.3k
views
File not found error on program installation.
samtools
htslib
Cpp
updated 5 days ago by
Ram
39k • written 3.6 years ago by
M.O.L.S
▴ 100
1
vote
10
replies
2.5k
views
How to specify/calculate subject coverage of the alignment (alignment of query[protein sequence] and subject[Nucleotide sequence]) in tBLASTn?
alignment
BLAST
tBLASTn
updated 1 day ago by
Ram
39k • written 4.2 years ago by
Kumar
▴ 100
0
votes
0
replies
987
views
FRMA processing on two different datasets of affy u133A not same dimensions
u133A
R
frma
affy
updated 1 day ago by
Ram
39k • written 4.2 years ago by
jmannhei
▴ 10
0
votes
0
replies
1.5k
views
CD-hit records matching and parsing
bash
python
cd-hit
text-processing
updated 1 day ago by
Ram
39k • written 4.2 years ago by
mnmalash
• 0
0
votes
0
replies
665
views
How to calculate the input-subtract signal for a specific enhancer region
next-gen-sequencing
ChIP-Seq
updated 1 day ago by
Ram
39k • written 4.2 years ago by
biofandd
• 0
1
vote
1
reply
1.3k
views
Can HISAT2 be invoked in bash shell, and can it be fed variables or names with wildcards as inputs?
Bash
Shell
HISAT2
updated 1 day ago by
Ram
39k • written 4.3 years ago by
RNAseqer
▴ 240
0
votes
3
replies
985
views
Explanation? Read depth, quality, and assembly accuracy in Methylome analysis context
Assembly
genome
methylation
updated 1 day ago by
Ram
39k • written 4.3 years ago by
davidfarr01
▴ 10
0
votes
0
replies
733
views
Data base or computational tool to help predict if two predicted interacting surface proteins are located on separate cells or on the same cell?
genome
RNA-Seq
updated 1 day ago by
Ram
39k • written 4.3 years ago by
charlesgwellem
• 0
1
vote
3
replies
751
views
Stratify phylogeny based on variables - e.g. which ST are represented by high % males
phylogeny
statistics
updated 1 day ago by
Ram
39k • written 4.3 years ago by
kalfsnes
▴ 10
0
votes
2
replies
926
views
what do you mean by segment pairs
rna
protein
updated 1 day ago by
Ram
39k • written 4.3 years ago by
a4appy23
▴ 50
0
votes
0
replies
629
views
Need open dataset of hydrocarbons in SMILE/ Chemfig/ Tex
latex
chemfig
smile
dataset
updated 1 day ago by
Ram
39k • written 4.3 years ago by
pgp14.aseem
• 0
0
votes
4
replies
2.1k
views
picard markduplicate output smaller file
picard
markduplicates
gatk
updated 1 day ago by
Ram
39k • written 4.3 years ago by
Peter Chung
▴ 190
0
votes
2
replies
1.7k
views
Fourfold degenerate codons in VCF File
vcf
genome
updated 1 day ago by
Ram
39k • written 4.4 years ago by
crippa.to
• 0
0
votes
0
replies
537
views
A way to compare genomic sequences with SNPs with sequences for allelic variants to identify genotype for an individual using Plink
snp
PLINK
alignment
sequencing
updated 1 day ago by
Ram
39k • written 4.4 years ago by
madeline.robinson
• 0
0
votes
0
replies
1.4k
views
envelope and alignment coordinates in hmmsearch result
hmmer
sequence
alignment
hmmsearch
updated 1 day ago by
Ram
39k • written 4.4 years ago by
sanjeet00001992
• 0
0
votes
1
reply
931
views
Questions about assembly of large metagenomics dataset
assembly
metagenomics
megahit
updated 2 days ago by
Ram
39k • written 4.5 years ago by
zorrilla
• 0
0
votes
0
replies
672
views
Brownian motion : Understanding the output of mvBM function.?
Phylogeny
Brownian
updated 2 days ago by
Ram
39k • written 4.5 years ago by
naveen_gabriel
• 0
2
votes
2
replies
765
views
Final year project query
project
updated 2 days ago by
Ram
39k • written 4.5 years ago by
talhar123456
• 0
1
vote
0
replies
1.2k
views
Align two single cell experiments
R
single-cell
updated 2 days ago by
Ram
39k • written 4.5 years ago by
elb
▴ 230
0
votes
3
replies
939
views
Sorting by Prefix Reversal (or Flipping Pancakes) approximation
algorithms
updated 2 days ago by
Ram
39k • written 4.5 years ago by
Gustavo Temple
• 0
3
votes
8
replies
1.7k
views
What is the minimum system requement for oxford nanopore read assembly
Assembly
updated 2 days ago by
Ram
39k • written 4.6 years ago by
nagendranp1991
• 0
0
votes
5
replies
941
views
Bioinformatics conference with possible publication
conference
updated 2 days ago by
Ram
39k • written 4.6 years ago by
bharata1803
▴ 550
1
vote
5
replies
1.3k
views
WGCNA Co-expression network analysis on cuffdiff output
wgcna
cuffdiff
updated 3 days ago by
Ram
39k • written 4.7 years ago by
sbb
▴ 10
1
vote
0
replies
1.2k
views
sequence alignment using edlib c++ library
cpp
alignment
updated 5 days ago by
Ram
39k • written 4.8 years ago by
BDK_compbio
▴ 130
119 results • Page
2 of 3
Recent Votes
Answer: Counting intronic reads in bulk RNA-seq
Answer: IGV displays genomic coordinates in a 1-based system or 0-based?
RNAseq expression data log2 transformed has negative values.
Samtools: "Too Many Open Files"
Filtering bad quality probes in illumina microarray data
gene filtering for agilent microarray using Limma
A: Identification Of Significant Differences Between Phylogentic Trees Using Distan
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Comment: Counting intronic reads in bulk RNA-seq
by
dsull
★ 4.2k
Correct, and I agree -- reads lying fully within introns are usually not counted for either single-cell or bulk. Inclusion of introns in a…
Answer: Counting intronic reads in bulk RNA-seq
by
swbarnes2
13k
Are you sure this is appropriate for bulk RNASeq? I thought intronic reads for single cell were only counted in nuclear preps.
Answer: Single cell chemistry
by
swbarnes2
13k
Are you sure these samples are 10x? How likey is it that the sequencing group messed up and ran the samples wrongly?
Comment: How to deal with duplicated gene IDs in TCGA RNA expression data?
by
Vincent Laufer
★ 2.8k
are they distinct transcript IDs but the same gene ID? can you provide any additional context?
Comment: SyntaxError (Perhaps you forgot a comma?) in snakefile when running FastQC.
by
Dhatri Badri
• 0
that didn't work either
Answer: Why are some WES VCFs larger than others?
by
Vincent Laufer
★ 2.8k
Hi @kermit and prash (and others)! Nice discussion. I wanted to offer some **biological rationales** in addition to the technical reasons …
Answer: SyntaxError (Perhaps you forgot a comma?) in snakefile when running FastQC.
by
WouterDeCoster
47k
There is no `:` after `rule fastqc`
Comment: SyntaxError (Perhaps you forgot a comma?) in snakefile when running FastQC.
by
Dhatri Badri
• 0
sorry that was a typo while i was copying my code! I still get the same error
Comment: too many zeros in 16S rRNA amplicon sequencing data
by
andres.firrincieli
3.3k
You have too many ASV (40k) and I think this is a problem related to the denoising (DADA2) of NovaSeq 6000 sequencing data. Maybe this post…
Answer: SyntaxError (Perhaps you forgot a comma?) in snakefile when running FastQC.
by
Pierre Lindenbaum
154k
> fastq.gz". what is the dot after `fastq.gz" ` ?
Comment: DownsampleSam
by
Pierre Lindenbaum
154k
1) I think this is just a warning 2) there must be another error displayed 3) look at samtools view --subsample 4) don't use loops but use…
Comment: ABySS genome assembler
by
npavliukovec
• 0
Hello, yes, I tried it, but I have to do my home work on university's remote computer, unfortunatelly I go an error, when I try to use abys…
Comment: desgin a primer for CDS
by
yuxiang
• 0
how can you know the primer is not bind to other gene site? how can you desgin an experiment? I use the FISH to identify the gene, how abo…
Comment: desgin a primer for CDS
by
yuxiang
• 0
sorry for my late reply, I am a student, my profossor ask me to dsgin a primer for the specific cDNA, I have solved now, thanks for your re…
Comment: vg: Mapping fewer reads to a genome graph than a linear reference
by
samuel.a.odonnell
▴ 470
In this case filtering for quality might help correct for this overattributing feature?
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