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1,000 results • Page
2 of 20
Sort: replies
Rank
Views
Votes
Replies
0
votes
12
replies
1.1k
views
Splitting CRAM files
CRAM-files
sequence-alignment
6 months ago by
langziv
▴ 30
1
vote
12
replies
1.2k
views
Volcano plot interpretation
EnhancedVolcano
volcano-plot
updated 3 months ago by
Ram
39k • written 23 months ago by
fahim
▴ 20
6
votes
12
replies
601
views
Help with error in cellranger
Cellranger
updated 21 days ago by
GenoMax
129k • written 22 days ago by
Chris
▴ 100
2
votes
12
replies
1.8k
views
Nothing will align with HTSeq?
RNA-Seq
htseq
updated 8 months ago by
Ram
39k • written 7.7 years ago by
Kristin Muench
▴ 620
1
vote
12
replies
3.2k
views
How to run multiple alignment and SNP-calling of WGS data in .gb and .fasta using Python or Ruby/Java or any free software?
alignment
sequencing
software
updated 11 months ago by
Ram
39k • written 8.2 years ago by
fashiondesignrussian
▴ 60
2
votes
12
replies
645
views
how to align an intron from a complex
genomic
updated 11 months ago by
WouterDeCoster
47k • written 11 months ago by
Bioinfo
• 0
2
votes
12
replies
4.2k
views
Adding barcodes to forward and reverse reads after sequencing
obitools
barcoding
next-gen-sequencing
updated 4 months ago by
Ram
39k • written 8.1 years ago by
cmogren
▴ 20
8
votes
12
replies
2.7k
views
Use BLAST Command Line Applications to run a folder of many sequences against a database
BLAST
updated 11 weeks ago by
Ram
39k • written 22 months ago by
daver.v
▴ 30
1
vote
12
replies
3.3k
views
dN/dS analysis of genomes
genome
sequence
alignment
7 months ago by
Mehmet
▴ 800
1
vote
12
replies
3.7k
views
Can anyone explain the weird Insert Size HIstogram
RNA-Seq
alignment
sequencing
updated 5 months ago by
ATpoint
72k • written 5.7 years ago by
SMILE
▴ 170
6
votes
12
replies
1.3k
views
VCF files 101 - for people from non Bioinformatics Background
vcf
sequencing
genome
variant-calling
updated 12 weeks ago by
Ram
39k • written 2.8 years ago by
akshaykum684
▴ 20
7
votes
12
replies
883
views
Integrated genes from bulk RNA seq and ATAC seq
bulk-RNA
integrated
ATAC-seq
updated 13 days ago by
Sasha
▴ 200 • written 19 days ago by
Chris
▴ 100
3
votes
12
replies
2.2k
views
What is NCBI Gene ID, where to find it and how to convert to entrez ID?
RNA-Seq
updated 5 days ago by
Pegasus
▴ 90 • written 3.7 years ago by
mnazir
▴ 10
5
votes
12
replies
651
views
Data from an experiment
single-cell
updated 3 months ago by
GenoMax
129k • written 3 months ago by
Chris
▴ 100
0
votes
12
replies
1.6k
views
bedtools intersect issue
bed
bedtools
updated 10 weeks ago by
Ram
39k • written 4.8 years ago by
elisheva
▴ 120
4
votes
12
replies
1.0k
views
Bulk RNA seq: all p adjusted are the same
p-adj
RNA-seq
differential-gene-expression
updated 5 months ago by
Ram
39k • written 12 months ago by
nils.simon.biology
▴ 10
0
votes
12
replies
2.9k
views
comparative analysis of two strains of bacteria's genomes
genome
gene
updated 20 days ago by
Ram
39k • written 5.6 years ago by
fonteneaudam
▴ 20
6
votes
12
replies
1.2k
views
Good tutorials/textbooks/articles to introduce biomarker discovery to a biologist?
r
biomarker
updated 11 weeks ago by
Ram
39k • written 4.4 years ago by
english.server
▴ 290
0
votes
12
replies
2.7k
views
Allpaths- Keep getting ConvertToFastbQualb.pl failed for group 'paired_ends' when I run PrepareAllPaths
next-gen
Assembly
updated 5 months ago by
Ram
39k • written 7.9 years ago by
mafireyi
▴ 80
2
votes
12
replies
1.4k
views
The best way to get gene lengths for 15K+ genes?
r
EDAseq
RNA-seq
8 months ago by
JACKY
▴ 100
0
votes
12
replies
2.3k
views
Tax4Fun2 - error
tax4fun
silva
blast
updated 9 months ago by
GenoMax
129k • written 15 months ago by
ymj
▴ 10
1
vote
11
replies
3.1k
views
bedtools fisher interpretation of "in -a" "not in -b"
fisher
bedtools
intersection
updated 3 months ago by
Ram
39k • written 5.3 years ago by
jomo018
▴ 720
4
votes
11
replies
6.6k
views
Correct way to calculate VAF (Variant allele fraction) from a VCF file
VCF
snp
9 months ago by
prasundutta87
▴ 650
8
votes
11
replies
1.4k
views
using STAR instead of HISAT2
STAR
updated 10 months ago by
Ram
39k • written 10 months ago by
Chris
▴ 100
6
votes
11
replies
929
views
Calculate RPKM
RPKM
11 weeks ago by
Chris
▴ 100
1
vote
11
replies
3.0k
views
merge samples in phyloseq returns NAs
R
phyloseq
biom
updated 7 months ago by
joe.e.weaver
• 0 • written 2.9 years ago by
annaA
▴ 10
0
votes
11
replies
890
views
Problem with Trimmomatic Multiple Paired-End sequencing.
Trimmomatic
updated 4 months ago by
GenoMax
129k • written 4 months ago by
john
• 0
5
votes
11
replies
6.4k
views
Error while running miso
RNA-Seq
splicing
updated 10 months ago by
Ram
39k • written 7.8 years ago by
priyankamaripuri
▴ 40
4
votes
11
replies
1.1k
views
Running STAR
STAR
10 months ago by
Chris
▴ 100
4
votes
11
replies
2.6k
views
7 follow
Getting coding sequence length
NCBI
Gene
CDS
updated 12 months ago by
newbio17
▴ 360 • written 2.9 years ago by
fi1d18
★ 4.2k
0
votes
11
replies
1.5k
views
Error in Importing data in qiime2
Metagenomics
Sequencing
Qiime2
Amplicon
10 months ago by
Vaishnavi
• 0
5
votes
11
replies
3.1k
views
Convert Plink to Arlequin
software-error
plink
Arlequin
PGDSpider
updated 12 weeks ago by
Ram
39k • written 5.1 years ago by
HG
▴ 30
0
votes
11
replies
927
views
Python - Samtools mpileup find snps with allele frequency
snp
mpileup
python
samtools
11 months ago by
pablosolar.r
▴ 20
4
votes
11
replies
2.7k
views
Please add an explicit type tag :NAME
software-error
next-gen
genome
updated 4 months ago by
Ram
39k • written 5.1 years ago by
mahdikhadem95
▴ 30
3
votes
11
replies
895
views
RepeatMasker error
repeatmasking
transciptome
RNA-seq
updated 11 months ago by
mark.ziemann
★ 1.8k • written 11 months ago by
barrypraveen
▴ 110
1
vote
10
replies
2.4k
views
Issue in running viroBlast from localhost
blast
php
viroBlast
javascript
sequence
updated 10 months ago by
Ram
39k • written 7.3 years ago by
arfaj a
▴ 10
3
votes
10
replies
987
views
Error with FindConservedMarkers()
FindConservedMarkers
3 months ago by
Chris
▴ 100
4
votes
10
replies
3.7k
views
TCGA normalized count data of 1000 samples for DGE
RNA-Seq
TCGA
updated 4 months ago by
Ram
39k • written 8.1 years ago by
David_emir
▴ 460
7
votes
10
replies
1.2k
views
col as names [solved]
R
updated 11 weeks ago by
Ram
39k • written 4.2 years ago by
demoraesdiogo2017
▴ 90
5
votes
10
replies
4.7k
views
Antisense transcription - how to detect it?
RNA-Seq
antisense
updated 9 months ago by
Ram
39k • written 7.7 years ago by
John
13k
0
votes
10
replies
2.3k
views
eXpress error gene length different
eXpress
rna-seq
updated 11 months ago by
Ram
39k • written 8.1 years ago by
bharata1803
▴ 550
2
votes
10
replies
3.2k
views
concatenate multiple GZip fastq files from multilane run and output combined gzip file
perl
fastqc
next-gen-sequencing
updated 10 months ago by
Ram
39k • written 7.5 years ago by
PAn
▴ 20
4
votes
10
replies
451
views
Extract unmapped reads OR reads covering chromosome 6 from a bam file?
fastq
bam
samtools
picard
3 months ago by
dps2501
▴ 20
5
votes
10
replies
434
views
Error when viewing a bam file
samtools
5 weeks ago by
Chris
▴ 100
0
votes
10
replies
2.0k
views
WGCNA, module trait relationship
R
updated 8 months ago by
priya.bmg
▴ 60 • written 2.8 years ago by
sadeghi.reyhane
• 0
5
votes
10
replies
932
views
How to change chromosome names in assembly fasta downloaded from NCBI?
grch38
ncbi
grch37
fasta
8 months ago by
magnolia
▴ 20
0
votes
10
replies
3.1k
views
6 follow
Error message running GeMoMa
gene
updated 9 months ago by
GenoMax
129k • written 3.9 years ago by
valopes
▴ 30
2
votes
10
replies
695
views
Can I directly compare the regions defined by peaks from pair-end 50 and pair-end 100 ATAC-seq?
ATAC-seq
updated 9 months ago by
ATpoint
72k • written 9 months ago by
Dan
▴ 120
1
vote
10
replies
2.6k
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 11 days ago by
Ram
39k • written 4.2 years ago by
Kumar
▴ 100
2
votes
10
replies
1.0k
views
Running salmon in alignment mode?
transcriptomics
salmon
metatranscriptomics
rna
rna-seq
11 months ago by
pearl2070
▴ 10
1,000 results • Page
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ChatGPT optimized for bioinformatics questions
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Answer: Extract sequences from a fastq file by a list of IDs
Answer: Extract sequences from a fastq file by a list of IDs
A: Collapse Repeated Reads
A: Extract Reads From A Bam File That Fall Within A Given Region
Comment: Masking before RNA-Seq Alignment and Gene Prediction in Plant Genomes
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Comment: Which method is the best for using in "dba.count" in Diffbind R package
by
Rory Stark
★ 1.7k
If you are calling `dba.normalize()` directly, it must be called *after* calling `dba.count()`. `dba.count()` will apply the default normal…
Comment: switching from illumination to NEB prep kits
by
GenoMax
129k
If you are simply replacing the library prep kit then it will be compatible with normal illumina libraries. If there is a different adapter…
Comment: How to use R installed by conda instead of it installed by apt on Ubuntu
by
Zhichao
• 0
yes, I have activated this conda environment. And the conda is in `PATH` . At first, I create a new conda environment `conda create -n ne…
Comment: Limma returned only positive logFC values
by
ATpoint
72k
Raw counts, raw meaning not manipulated by any transformation. See limma and edgeR manual, it clearly covers that for using limma-trend and…
Comment: Alternative To interactions comparison in limma in DESeq2
by
ATpoint
72k
https://support.bioconductor.org/p/9143932/ -- see the lower parts where Michael Love answers, it comes down to numeric contrasts.
Comment: Limma returned only positive logFC values
by
melissachua90
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The `mat` is log2-normalized raw data. Is it feasible? Or should I feed in counts?
Comment: DESeq2 for different design and normalized counts
by
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Nope, please read the manual of DESeq2, it clearly tells to use raw counts. What "normalized counts" do you have exactly? limma-trend might…
Comment: How to use R installed by conda instead of it installed by apt on Ubuntu
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72k
Did you activate your conda environment? Is conda in `PATH`? Please describe what you did.
Comment: Limma returned only positive logFC values
by
ATpoint
72k
Bottom line is, if you are using an intercept-free model (that is what `~0+...` is doing) then you have to use contrasts. In a "normal" mod…
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Thanks for sharing ! It seems there is a problem to install on Kaggle cloud (like a Colab): I tried several ways: https://www.kaggle.com/co…
Comment: Masking before RNA-Seq Alignment and Gene Prediction in Plant Genomes
by
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4.4k
I am not sure what you gain by using hard masked genome for RNA-Seq mapping. There will be reads covering some introns. But if you mask rep…
Comment: Extract sequences from a fastq file by a list of IDs
by
mhpakdel96
• 0
Thanks a lot, it works
Comment: Differential protein expression analysis
by
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I don't have a tutorial but see this paper I co-authored: https://pubs.acs.org/doi/abs/10.1021/acs.jproteome.0c00666 All of the upstream …
Comment: Differential protein expression analysis
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Ribo
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Thank you! Is there a recommended tutorial for proteomics analysis?
Comment: Limma returned only positive logFC values
by
melissachua90
▴ 40
I clustered the samples into subtypes and am now comparing the differential expression across the subtypes.
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