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Limit : this month
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683 results • Page
1 of 14
Sort: replies
Rank
Views
Votes
Replies
76
votes
72
replies
20k
views
19 follow
Tutorial:
Clustering of DAVID gene enrichment results from gene expression studies
enrichment
david
24 days ago by
Kevin Blighe
88k
29
votes
28
replies
34k
views
11 follow
Split Fastq Files Into Chunks Of 1M Reads
split
fastq
updated 16 days ago by
thomas.heigl.ibk
• 0 • written 12.8 years ago by
Bioscientist
★ 1.7k
38
votes
24
replies
2.3k
views
10 follow
NGS forensics: how to know if data is fabricated
fastq
STAR
NGS
Illumina
updated 18 days ago by
i.sudbery
19k • written 21 days ago by
noodle
▴ 580
9
votes
23
replies
9.8k
views
Tool:
BioLabDonkey - new Mac program for molecular biologists
software
biolabdonkey
7 days ago by
vytarasov
▴ 180
7
votes
16
replies
958
views
How many reads for WGS Sequencing?
WGS
Bacterial-Genomics
19 days ago by
Ruqaiya
• 0
34
votes
16
replies
21k
views
9 follow
Filtration Of Reads With Length Lower Than 30 From Bam
read
length
bam
updated 29 days ago by
Hagen
▴ 10 • written 10.3 years ago by
filipzembol
▴ 180
8
votes
16
replies
1.2k
views
How to convert plink files to Hapmap Format
GWAS
Plink
updated 22 days ago by
bk11
★ 2.5k • written 10 weeks ago by
Sofia
• 0
1
vote
16
replies
726
views
Blastn error : ncbi::CObject::ThrowNullPointerException() - Attempt to access NULL > pointer.
blast
ncbi
updated 15 hours ago by
GenoMax
142k • written 3 days ago by
hophuquy0944
• 0
10
votes
16
replies
17k
views
7 follow
How Can I Count Snps In My Final Vcf Files
SNP
updated 11 days ago by
Pierre Lindenbaum
161k • written 5.8 years ago by
mostafarafiepour
▴ 180
4
votes
15
replies
1.7k
views
how to test for differential expression in samples where a global increase in gene expression is expected
edgeR
DESeq
Differential-Expression
RNA-Seq
updated 15 days ago by
Gordon Smyth
★ 7.2k • written 5 months ago by
raplayer
▴ 10
10
votes
14
replies
797
views
6 follow
Bacterial plasmid analysis
bacteria
plasmid
wgs
hybridassembly
sequencing
updated 11 days ago by
GenoMax
142k • written 17 days ago by
nicole.kavanagh
• 0
1
vote
14
replies
2.5k
views
Extract gRNA sequence using cutadapt
cutadapt
trimming
crispr
sequencing
updated 16 days ago by
GenoMax
142k • written 4.5 years ago by
Swimming bird
▴ 20
2
votes
14
replies
3.0k
views
6 follow
CNVKIT - unable to produce scatter and diagram pdfs
cnvkit
updated 4 days ago by
Anitha
• 0 • written 4.8 years ago by
ww22runner
▴ 60
13
votes
14
replies
958
views
High Malat-1 expression in single cell data
single-cell
updated 11 days ago by
t.montserrat.ayuso
▴ 40 • written 19 days ago by
carolofharvest
▴ 40
9
votes
13
replies
4.8k
views
Custom Reference panel creation for data imputation from .vcf files
imputation
reference panel
updated 8 days ago by
analyst
▴ 50 • written 6.4 years ago by
David_emir
▴ 490
5
votes
13
replies
2.0k
views
Tutorial:
Installing/switching between versions of R/Rstudio/Bioconductor on personal machine (Linux | Ubuntu)
R
Ubuntu
Linux
Bioconductor
Rstudio
updated 28 days ago by
ATpoint
82k • written 29 days ago by
BioinfGuru
★ 1.7k
0
votes
13
replies
3.6k
views
6 follow
Tax4Fun2 - error
tax4fun
silva
blast
updated 24 days ago by
drstalinantony28
• 0 • written 2.3 years ago by
ymj
▴ 10
4
votes
12
replies
4.9k
views
10 follow
How to analyze Infinium Mouse Methylation BeadChip array data?
Methylation
Experience
Illumina
Mouse
updated 9 days ago by
Tawny
▴ 180 • written 3.0 years ago by
julia_geh
▴ 20
38
votes
12
replies
31k
views
9 follow
How to systematically check if a bam file is truncated
Exomeseq
updated 1 day ago by
alanh
▴ 170 • written 7.1 years ago by
jonessara770
▴ 240
16
votes
12
replies
7.5k
views
10 follow
how to split multi-fasta file into single fasta file named by header
genome
perl
python3
bash
python
updated 15 days ago by
rsieber
▴ 10 • written 3.2 years ago by
Kumar
▴ 120
19
votes
11
replies
14k
views
10 follow
How Can We Find The Info For 3'Utr And 5'Utr In Gencode Gtf File?
utr
updated 22 days ago by
cmdcolin
★ 3.8k • written 10.8 years ago by
J.F.Jiang
▴ 920
1
vote
11
replies
5.6k
views
Truncated Bam Error
R
next-gen
sequencing
software error
updated 13 days ago by
guanghao
• 0 • written 6.2 years ago by
vivekruhela
▴ 20
25
votes
11
replies
3.8k
views
6 follow
Forum:
Site Use Guidelines
meta
biostars
Guidelines
updated 25 days ago by
Ram
43k • written 14.6 years ago by
Istvan Albert
100k
2
votes
11
replies
1.0k
views
Questions about a bug when transferring cram file to bam file
sequence
samtools
bcftools
updated 19 days ago by
jkbonfield
★ 1.2k • written 4 weeks ago by
me
• 0
4
votes
11
replies
896
views
Redirection of Duplicate PMIDs
pubmed
pmid
updated 25 days ago by
LauferVA
4.2k • written 26 days ago by
dominickd
• 0
0
votes
11
replies
719
views
How do I use the STARSolo aligner with MGI DNBelab C series HT scRNAseq libraries?
STARSolo
scRNA-seq
STAR
snRNA-seq
MGI
23 days ago by
atowns21
• 0
2
votes
11
replies
698
views
DEG analysis with limma and contrast matrix using multiple Parkinson's cohorts in whole blood: is it normal to always get NS?
rstudio
DEG
limma
1 day ago by
egascon
• 0
0
votes
11
replies
550
views
In IGV is this a heterogeneous mutation or false call?
mutations
IGV
heterogeneous
6 days ago by
Tuck898
• 0
0
votes
10
replies
641
views
Low mapping rate with Salmon
RNA-seq
Salmon
Quantification
updated 18 days ago by
i.sudbery
19k • written 26 days ago by
Patadu94
• 0
40
votes
10
replies
43k
views
8 follow
Batch effects : ComBat or removebatcheffects (limma package) ?
limma
sva
Combat
batch-effect
updated 19 days ago by
cwwong13
▴ 40 • written 6.8 years ago by
lessismore
★ 1.3k
1
vote
10
replies
896
views
error to run rnammer
phylogenomics
rRNA_extraction
rnammer
updated 13 days ago by
antonio.spl
• 0 • written 4 months ago by
microorganism_001
▴ 30
1
vote
10
replies
1.1k
views
Troubleshooting RNA-seq data with DNA contamination
RNA-seq
DESeq2
DNA-contamination
24 days ago by
DKA
▴ 40
4
votes
9
replies
2.2k
views
6 follow
Same sequencing sample in multiple lanes. How to analyse it?
sequencing
bowtie2
alignment
samtools
ngs
updated 15 days ago by
ST
• 0 • written 2.2 years ago by
Federico
• 0
0
votes
9
replies
1.5k
views
kinannote software installation problems
kinannote
updated 10 days ago by
Emanoelle
• 0 • written 5.8 years ago by
Elizabeth
▴ 30
4
votes
9
replies
2.7k
views
Tool:
CANEapp, a user-friendly application for automated next generation transcriptomic data analysis
RNA-Seq
written 8.3 years ago by
dvelmeshev
• 0
1
vote
9
replies
407
views
UMI-Tools knee-method has great influence on the results of white list
single-cell
whitelist
UMI
RNA
UMI-Tools
updated 8 days ago by
i.sudbery
19k • written 11 days ago by
Assa Yeroslaviz
★ 1.8k
3
votes
9
replies
629
views
Is it Acceptable to Have Uniform Quality Scores in a FASTQ File?
FASTQ
updated 24 days ago by
Istvan Albert
100k • written 26 days ago by
Κοσμάς
• 0
2
votes
9
replies
710
views
Filtering Multi-sample VCF file for all except one Genotype
variant
SNP
VCF
updated 3 days ago by
Pierre Lindenbaum
161k • written 11 days ago by
schmince
• 0
2
votes
9
replies
944
views
TCGA2STAT Error: Firehose connection
FIREHOSE
TCGA
updated 25 days ago by
LauferVA
4.2k • written 7 months ago by
Gnana
• 0
4
votes
9
replies
2.1k
views
Legend and hap files for imputation with 38 build
reference
38build
impute
imputation
19 days ago by
anna
▴ 20
0
votes
9
replies
358
views
Duplicated reads (IDs) from nanopore sequencing
bam
nanopore
sequencing
3 days ago by
njornet
▴ 20
0
votes
9
replies
605
views
Using VEP annotation output as the input for a second VEP annotation
Annotation
VEP
VCF
3 days ago by
Arton
▴ 10
4
votes
9
replies
447
views
Faster Needleman-Wunsch rapid global alignment of two sequences?
Needleman-Wunsch
alignment
1 day ago by
Gabriel R.
★ 2.9k
0
votes
9
replies
617
views
Applying the metacell2 algorithm using python
python
single-cell
scanpy
metacell2
updated 3 days ago by
Wayne
★ 2.0k • written 12 days ago by
JACKY
▴ 140
0
votes
9
replies
2.6k
views
6 follow
Cannot process all the reads in a fast5 file?
metagenome
base-calling
fastq
nanopore
updated 20 days ago by
Ram
43k • written 9 months ago by
Gio
• 0
3
votes
8
replies
624
views
How to access TCGA samples that were treated with a specific drug?
TCGA
RNA-seq
12 days ago by
Qroid
▴ 40
1
vote
8
replies
958
views
Adding CB tag to bam file
samtools
bam
updated 23 days ago by
Pierre Lindenbaum
161k • written 4 weeks ago by
Maria
• 0
0
votes
8
replies
472
views
Error in cnetplot enrichplot package
R
updated 26 days ago by
Ram
43k • written 26 days ago by
Farhad
• 0
0
votes
8
replies
463
views
Different output for read length
samtools
BAM
9 days ago by
marco.barr
▴ 130
3
votes
8
replies
1.4k
views
Cellranger count error: Input FASTQ file ended prematurely
scRNA-seq
Cellranger
STARsolo
10X
updated 28 days ago by
swbarnes2
14k • written 9 months ago by
bp22
▴ 80
683 results • Page
1 of 14
Recent Votes
A: How is the design in DESeq2 work?
Error in CIBERSORTx ($ operator is invalid for atomic vectors)
Answer: RNAseq coverage vs depth for transcript isoform expression?
constructing pangenome through psvcp
Differential Expression with limma: Contrast and Design Matrix, combinatorial approach valid?
Differential Expression with limma: Contrast and Design Matrix, combinatorial approach valid?
Answer: RNAseq coverage vs depth for transcript isoform expression?
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Answer: CellRanger output more cells than specified using --force-cells? Why?
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▴ 30
I actually had this same issue with CellRanger v7- turns out that since you have 2 species in your mapping reference, CellRanger is forcing…
Answer: Checking chromosome builds for genotyping data
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Muhammad
• 0
Assume you have genotype data in Plink format. (G.bed, G.bim, G.fam) Download some reference panel data in Plink format (R.bed, R.bim, R.f…
Comment: Error in CIBERSORTx ($ operator is invalid for atomic vectors)
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did you ever figure it out? i'm having the same issue.
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Hi Larissa! I am the lead developer of R2DT and I've just noticed this question. Could you please email help@r2dt.bio with your input seque…
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Fixed the issue by updating nucmer version.
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142k
Can you create a small test database (`makeblastdb`) from your query file and try to run the search against the same file and see if that w…
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you can `dput(head(df)` for the both the data frame so that other can test for possible solutions
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What is your question? It's unclear.
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One question before offering more solutions: are you trying to learn Python with this as an example problem, or are you trying to find the …
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See the exploration of isoform estimation precision vs read length and sequencing depth in our paper: https://doi.org/10.1093/nar/gkad1167.…
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txema.heredia
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Why does the tool require gene symbols and not ensembl ids? Is it retrieving information from somewhere else? If so, your best bet is to fi…
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mavy
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Thank you so much for your response . Really appreciate it. I will try the way you mentioned and will get back if I have any query
Comment: Blastn error : ncbi::CObject::ThrowNullPointerException() - Attempt to access NU
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hophuquy0944
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i have the same error, i used high performance computer, here is my code to set memory. srun --nodes=1 --ntasks=1 --cpus-per-task=24 -…
Comment: Overlapping Ranges within Granges object
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Yes, `bedmap` will perform operations on one or two BED files.
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Apologies for resurrecting this post, but any idea what that functions "regions" paramater takes? Would it be a GRanges object? The documen…
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