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1,000 results • Page
1 of 20
Sort: Rank
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Views
Votes
Replies
0
votes
0
replies
18
views
WGCNA: many over and under-expressed features in modules of a signed network
WGCNA
40 minutes ago by
Sebastian Hesse
▴ 320
0
votes
2
replies
23
views
Docker Error while running nf-core/rnaseq pipeline
rnasequencing
nf-core
docker
updated 15 minutes ago by
GenoMax
129k • written 1 hour ago by
eesha28112001
• 0
0
votes
1
reply
19
views
sctransform on scRNA seq
seurat
updated 44 minutes ago by
ATpoint
72k • written 53 minutes ago by
friguiahlem8
▴ 10
1
vote
2
replies
36
views
What type of normalization did they use in this article?
log
normalization
TPM
r
15 minutes ago by
JACKY
▴ 90
0
votes
0
replies
10
views
Impute haplotypes (ImputePipelinePlugin) execution error - PHG
phg
1 hour ago by
jrodrigu
• 0
0
votes
3
replies
33
views
MACS2 peak calling
MACS2
peak
calling
updated 44 minutes ago by
ATpoint
72k • written 1 hour ago by
Maurice
• 0
0
votes
1
reply
70
views
Which type of variant caller should I use in a WES normal cell line sample?
variant-caller
WES
updated 1 hour ago by
ATpoint
72k • written 8 hours ago by
bompipi95
▴ 120
1
vote
2
replies
52
views
Alignment of case vs. control from different origin
Alignment
RNAseq
updated 17 minutes ago by
ATpoint
72k • written 3 hours ago by
sativus
• 0
0
votes
2
replies
182
views
Peaks annotation on bacterial genome
ChIPpeakAnno
annotation
bacteria
1 hour ago by
Maurice
• 0
0
votes
1
reply
29
views
Create customized gene annotation file
reference
mkref
genome
cellranger
updated 1 hour ago by
ATpoint
72k • written 2 hours ago by
rhonddaskl
• 0
0
votes
0
replies
21
views
metagenomics data - AMR genes
amr
resistome
resistance
ARG
metagenomics
2 hours ago by
aziznasr1920
• 0
0
votes
1
reply
32
views
How to get a comperative result of 2 bed files?
bam
cnv
bed
updated 1 hour ago by
Pierre Lindenbaum
154k • written 2 hours ago by
herh
• 0
0
votes
0
replies
28
views
1000G reference panel for LD clumping
LD
3 hours ago by
en_keser
• 0
6
votes
25
replies
29k
views
14 follow
CluserProfiler message "No gene can be mapped"
R
updated 4 hours ago by
13554221497
• 0 • written 5.2 years ago by
ARich
▴ 130
160
votes
63
replies
76k
views
38 follow
Selecting Random Pairs From Fastq?
random
fastq
sequence
illumina
code
updated 4 hours ago by
sebastian.gregoricchio
▴ 30 • written 12.2 years ago by
Ketil
4.1k
4
votes
5
replies
13k
views
Take A Subset Of A Fastq Paired-End Sample
fastq
illumina
paired-end
reads
rnaseq
rna-seq
updated 4 hours ago by
sebastian.gregoricchio
▴ 30 • written 10.2 years ago by
dfernan
▴ 730
0
votes
1
reply
67
views
Forum:
Colleges
bioinformatics
universities
Colleges
india
updated 4 hours ago by
WouterDeCoster
47k • written 4 hours ago by
mahimanepalli36
• 0
1
vote
3
replies
113
views
Concatenating text files based on common indices
Bash
Genetics
Genes
Bioinformatics
Python
updated 4 hours ago by
Mensur Dlakic
★ 23k • written 7 hours ago by
Hau Tak Leighton
• 0
0
votes
7
replies
290
views
how to create correlation matrix R
pearson-correlation
R
updated 7 hours ago by
seidel
11k • written 1 day ago by
satva72
• 0
0
votes
0
replies
52
views
Nucleotide alignments from mmseqs "tblastn"
mmseqs2
tblastn
mmseqs
10 hours ago by
saladi1
▴ 30
3
votes
4
replies
250
views
I don't want to believe the Interproscan DB estimated download time.
Interproscan
updated 11 hours ago by
Mensur Dlakic
★ 23k • written 1 day ago by
gh
• 0
2
votes
2
replies
244
views
What is the best way to clean bulk RNA-seq data?
normalization
TPM
r
updated 15 hours ago by
swbarnes2
13k • written 1 day ago by
JACKY
▴ 90
0
votes
1
reply
149
views
Make a BedGraph file
BedGraph
RepeatMasker
BED
updated 15 hours ago by
bhumm
▴ 40 • written 1 day ago by
kirillkirilenko
▴ 10
1
vote
7
replies
212
views
RNAseq Data and Pipeline
RNA-Seq
DESeq2
Differential-Gene-Expression
updated 16 hours ago by
Ram
39k • written 16 hours ago by
turcoa1
• 0
0
votes
2
replies
578
views
ERROR running Cuffmerge in reference based RNA-SEQ analysis?
cuffmerge
RNA-Seq
Cufflinks
updated 17 hours ago by
Ram
39k • written 12 months ago by
Meeran
• 0
0
votes
7
replies
494
views
How to deal with duplicated gene IDs in TCGA RNA expression data?
TCGA
Expression
mRNA
updated 8 hours ago by
Vincent Laufer
★ 2.8k • written 4 days ago by
Camilo Andres
▴ 30
0
votes
2
replies
99
views
gatk Hardfilter Error
hardfilter
updated 18 hours ago by
Pierre Lindenbaum
154k • written 18 hours ago by
bestone
▴ 10
0
votes
3
replies
153
views
How to make a dotplot for bulk RNA average expression ?
Dotplot
RNA-seq
updated 11 hours ago by
bhumm
▴ 40 • written 19 hours ago by
LionisOne
• 0
0
votes
2
replies
111
views
Dada2 in Qiime2: losing reads during merging
Qiime2
Chimer
Dada2
3 hours ago by
kamanovae
▴ 80
0
votes
1
reply
122
views
NCBI Common Taxonomy Tree
phylogenetic-tree
comparative-taxonomy
ncbi
updated 16 hours ago by
GenoMax
129k • written 19 hours ago by
fafad046
• 0
3
votes
6
replies
217
views
Salmon Index
transcriptomics
Bulk
RNA-sequencing
updated 16 hours ago by
GenoMax
129k • written 19 hours ago by
ashleymb1116
• 0
1
vote
4
replies
530
views
Expected number of haplotype IDs per path in PHG
PHG
updated 19 hours ago by
Ram
39k • written 5 weeks ago by
twrl8
• 0
0
votes
2
replies
120
views
minimap's SAM file MAPQ value for the unique alignments
minimap
MAPQ
RNAseq
updated 4 hours ago by
WouterDeCoster
47k • written 21 hours ago by
Mohd
• 0
0
votes
2
replies
99
views
sorting BAM file
BAM
updated 1 hour ago by
ATpoint
72k • written 21 hours ago by
Mohammad Amin
• 0
0
votes
1
reply
80
views
Search SRA metadata for Histological_Type and Body_Site
sra
updated 21 hours ago by
GenoMax
129k • written 22 hours ago by
oakhamwolf
▴ 20
2
votes
3
replies
195
views
NCBI refseq ids to uniprot ids
refseq
Uniprot
updated 14 hours ago by
Ram
39k • written 1 day ago by
t.ali
• 0
1
vote
3
replies
131
views
Covert multiple short sequence into list of IUPAC motif
sequence
updated 21 hours ago by
GenoMax
129k • written 23 hours ago by
praasu
▴ 40
1
vote
0
replies
76
views
Resequencing data of pangenome
NGS
PanGenome
Resequence
updated 16 hours ago by
Ram
39k • written 1 day ago by
bioinfo223
▴ 10
3
votes
2
replies
165
views
Graphing Average Expression of Group of Genes
Boxplot
R
updated 19 hours ago by
Shred
★ 1.2k • written 1 day ago by
cthangav
▴ 40
0
votes
0
replies
66
views
Converting rds file to h5ad and saving raw counts as X
R
seurat
updated 1 day ago by
zx8754
11k • written 1 day ago by
sidrah.maryam
▴ 50
0
votes
1
reply
125
views
Seurat: How to get all genes name of a cell ?
seurat
updated 13 hours ago by
jv
★ 1.2k • written 1 day ago by
Picasa
▴ 640
1
vote
0
replies
171
views
miRDeep2 installation showing "ln: failed to create symbolic link './randfold': File exists" error.
miRDeep2
updated 14 hours ago by
Ram
39k • written 1 day ago by
Supernova
• 0
0
votes
0
replies
88
views
Bulk RNA sequencing time course pathway analysis progression visualization
time-course
RNA-seq
pathway
updated 21 hours ago by
Ram
39k • written 1 day ago by
Fred
• 0
0
votes
1
reply
254
views
CORUM server not working?
corum
protein
complexes
database
updated 1 day ago by
Elisabeth Gasteiger
★ 2.2k • written 11 days ago by
marta
• 0
0
votes
0
replies
103
views
Job:
PhD students in Data Science - DTU Biosustain
PhD
Biology
Data-Science
updated 16 hours ago by
Ram
39k • written 1 day ago by
info
▴ 70
0
votes
3
replies
227
views
1000G reference panel for LD
plink
gwas
LD
1 day ago by
en_keser
• 0
0
votes
1
reply
130
views
How to calculate SARS-2'S evolutionary rate
evolutionary-rate
updated 20 hours ago by
Ram
39k • written 1 day ago by
chengc2016zzu
• 0
3
votes
4
replies
187
views
how to use nohup with parallel
parallel
nohup
updated 23 hours ago by
GenoMax
129k • written 1 day ago by
gavin
• 0
0
votes
0
replies
81
views
Michigan Imputation Server - Local docker image
genotype
WGS
imputation
1 day ago by
batch_effect
• 0
1
vote
1
reply
124
views
How do I restrict to only hm3 SNPs for plink analyses?
plink
hm3
updated 1 day ago by
chrchang523
10k • written 1 day ago by
garrett.ennis
• 0
1,000 results • Page
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Recent Votes
Answer: Alignment of case vs. control from different origin
What type of normalization did they use in this article?
Answer: I don't want to believe the Interproscan DB estimated download time.
C: removing overrepresented sequences from rna-seq
C: removing overrepresented sequences from rna-seq
C: Filtering rRNA contamination (indicated by GC content plots) from RNA-seq data
Answer: Any methods available to do QC analysis of Pacbio raw data??
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Recent Replies
Comment: What type of normalization did they use in this article?
by
JACKY
▴ 90
I see, do you think there is any way to retrieve the uncorrected TPM data? can I undo the corrections and scalings applied to the data?
Comment: Alignment of case vs. control from different origin
by
ATpoint
72k
I would not even do the trimming. Any differential analysis of case (normal/control) versus anything in TCGA (progressed cancer) is going t…
Comment: Docker Error while running nf-core/rnaseq pipeline
by
eesha28112001
• 0
How do I do that?
Comment: MACS2 peak calling
by
ATpoint
72k
You do not need strand information for this as, as I said, strands do not apply in DNA-seq.
Answer: Docker Error while running nf-core/rnaseq pipeline
by
ATpoint
72k
> read-only file system You must make sure that the output destination is writable.
Answer: sctransform on scRNA seq
by
ATpoint
72k
No, there is no magic to make data appear where previously there were none.
Answer: What type of normalization did they use in this article?
by
Matthias Zepper
3.7k
> Transcriptomic analysis > > [...] We subsequently filtered genes that > were not expressed in any of the samples (in each cohort > indep…
Comment: How to get a comperative result of 2 bed files?
by
Pierre Lindenbaum
154k
what kind of measurement do you need ? I see one bed file in your description , what are the TWO bed file ?
Comment: MACS2 peak calling
by
Maurice
• 0
Thank you! And for what regards peaks annotation, how can the tool I'm going to use assign peaks to the correct location without knowing t…
Comment: sorting BAM file
by
ATpoint
72k
You can simply use `samtools sort` to get rid of this read group nonsense these Broad institute tools always complain about.
Answer: Which type of variant caller should I use in a WES normal cell line sample?
by
ATpoint
72k
Any variant caller will do. Somatic calling is usually an additional mode while calling without matched normal is typically always possible.
Comment: Create customized gene annotation file
by
ATpoint
72k
Plese confirm whether you read and tried the manual: https://support.10xgenomics.com/single-cell-gene-expression/software/pipelines/latest/…
Answer: MACS2 peak calling
by
ATpoint
72k
Yes, that is correct. Peaks from experiments such as ChIP-seq or ATAC-seq are based on DNA, which is double-stranded and unlike RNA (where …
Answer: Alignment of case vs. control from different origin
by
i.sudbery
17k
I hate to be the one to tell you this, but the reason you have been unable to find an answer isnthat what you are trying to do is not gener…
Answer: Peaks annotation on bacterial genome
by
Maurice
• 0
Thank you for your kind reply! I have just a further question. Which is the difference between using annoPeaks and annotatePeaksinbatch wi…
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