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122,217 results • Page
719 of 2445
Sort: Rank
Rank
Views
Votes
Replies
2
votes
2
replies
1.0k
views
VCF keep only genotyped positions
vcf
genotype
snp
4.8 years ago by
sahahig469
▴ 10
0
votes
2
replies
976
views
compare a list of RNA with RNA sequence in RFAM using python
RNA-Seq
RFam
Python
4.8 years ago by
phangou10
• 0
0
votes
0
replies
653
views
Duplicates probability depending on the number of flow cells
next-gen
sequencing
duplicates
4.8 years ago by
kseniya.petrova
• 0
0
votes
7
replies
1.8k
views
deseq2 design with two variables
deseq2
design
4.8 years ago by
biosjm
• 0
2
votes
1
reply
1.1k
views
Is OMA suitable for prediction of GO function in metagenomic datasets?
OMA
GO_Label
updated 4.8 years ago by
clement.train
▴ 60 • written 4.9 years ago by
crl111222
▴ 10
0
votes
4
replies
1.5k
views
Oligo algorithm analyzer
oligo analyzer
primer
4.8 years ago by
anasofiamoreira94
▴ 80
2
votes
3
replies
1.4k
views
How to convert gff3 format, PASApipeline
RNA-Seq
Assembly
updated 4.8 years ago by
Juke34
9.3k • written 4.8 years ago by
Ruixuan
• 0
1
vote
11
replies
2.5k
views
ground truth dataset for BAM read counts
genome
alignment
read counts
ground truth
4.8 years ago by
Marius
▴ 30
1
vote
1
reply
1.1k
views
Splice junction coordinates for Ensembl transcripts
Ensembl
Splicing
Annotation
updated 4.8 years ago by
Emily
24k • written 4.8 years ago by
AJ_S
• 0
8
votes
3
replies
1.6k
views
how to select features for high dimension data?
machine-learning
updated 2.1 years ago by
Ram
45k • written 4.8 years ago by
pt.taklifi
▴ 70
16
votes
10
replies
8.5k
views
from txt to bed
ChIP-Seq
updated 4.8 years ago by
Biostar
20 • written 8.7 years ago by
dimitrischat
▴ 210
0
votes
0
replies
418
views
Mitochondrial genome sequence
sequencing
4.8 years ago by
ganesh_swamy2005
• 0
3
votes
9
replies
3.9k
views
Ubuntu 20.04.1 for genomic data analysis
next-gen
sequencing
genome
updated 4.8 years ago by
tothepoint
▴ 940 • written 4.8 years ago by
Alireza.Tafazoli
• 0
1
vote
0
replies
1.2k
views
Job:
Postdoctoral fellow -- genetic/molecular epidemiology
multiomics
data-analysis
updated 2.5 years ago by
Ram
45k • written 4.8 years ago by
zwangmanu
▴ 10
3
votes
5
replies
4.5k
views
Post-imputation QC GWAS analysis
GWAS
Rstudio
Imputation
TopMed
updated 4.8 years ago by
Biostar
20 • written 5.2 years ago by
AR
• 0
0
votes
1
reply
1.2k
views
Trimming Illumina Seq with TRIMMOMATIC
trimmomatic
GBS
Illumina
4.8 years ago by
giulia.trauzzi
▴ 30
0
votes
2
replies
1.3k
views
bedtools genomecov max function not working correctly
Assembly
bedtools
genomecov
updated 2.5 years ago by
Ram
45k • written 4.8 years ago by
RBright21
▴ 10
4
votes
2
replies
6.5k
views
problems installing HTSeq
RNA-Seq
HTSeq
DEXSeq
updated 4.8 years ago by
Biostar
20 • written 8.6 years ago by
Lila M
★ 1.3k
1
vote
2
replies
2.0k
views
GSEA with GGProfiler2 (?"annotated" vs "known" for background control)
RNA-Seq
GSEA
GGProfiler2
updated 4.8 years ago by
ATpoint
90k • written 4.8 years ago by
drodavis0
• 0
0
votes
0
replies
702
views
database about population data of aquatic animal organisms
databases
4.8 years ago by
eridanus
▴ 40
0
votes
0
replies
690
views
Can I do microarray meta-analysis combinning Induced pluripotent stem cells and neurons?
R
geno
4.8 years ago by
firstorthopedicdoctor
▴ 30
2
votes
2
replies
2.0k
views
Merging PacBio and Nanopore reads
Nanopore
Pacbio
next-gen
long reads
Assembly
updated 4.8 years ago by
harishk0201
▴ 140 • written 4.8 years ago by
Sbrillo
▴ 10
2
votes
7
replies
4.1k
views
Finding assembled transcript sequences from StringTie output
RNA-Seq
StringTie
Assembled Transcripts
Sequences
4.8 years ago by
Jen
▴ 100
2
votes
3
replies
950
views
ENCODE terminology question
sequencing
alignment
updated 4.8 years ago by
i.sudbery
22k • written 4.8 years ago by
ccc
▴ 30
0
votes
5
replies
2.0k
views
MEgene correlated to triat and Gene signficance coorelated to triat
WGCNA
andres.firrincieli
updated 4.6 years ago by
eggerj
▴ 40 • written 4.8 years ago by
adR
▴ 130
0
votes
4
replies
1.4k
views
Identify contaminants in my transcriptomic sequences
Assembly
transcriptome
de-novo
updated 4.8 years ago by
GenoMax
154k • written 4.8 years ago by
Rogerio Ribeiro
▴ 110
0
votes
1
reply
898
views
where to download proprietary miRNA software
mirna
updated 4.8 years ago by
Michael
56k • written 4.8 years ago by
972050141
• 0
0
votes
2
replies
794
views
whole genome sequencing data analysis
Assembly
updated 4.8 years ago by
Biostar
20 • written 4.8 years ago by
ipb727258
• 0
0
votes
3
replies
1.1k
views
snp list from Affymetirx microarray files
SNP
Affymetrix
R
4.8 years ago by
avichaireich
▴ 10
0
votes
2
replies
1.1k
views
error when running "SeuratToExpressionSet"
SeuratToExpressionSet
Seurat
4.8 years ago by
Laven9
• 0
0
votes
1
reply
3.5k
views
GATK tool to merge INDEL with SNPs with the same set of samples
VCF
GATK
updated 4.8 years ago by
Biostar
20 • written 4.8 years ago by
MAPK
★ 2.1k
0
votes
5
replies
1.2k
views
Pair ended samples cannot map to the genome
ChIP-Seq
4.8 years ago by
SayHey
• 0
0
votes
1
reply
721
views
Problem uploading reference database silva_123 for 16S V3-4 analysis
alignment
4.8 years ago by
arturo.gonzales
• 0
1
vote
1
reply
2.8k
views
How to interpret highly variable genes plot in Scanpy?
python
single-cell RNA Seq
updated 2.8 years ago by
mt_pereira
• 0 • written 4.8 years ago by
Pratik
★ 1.1k
1
vote
3
replies
3.1k
views
psmc bootstrapping help
bootstrap
psmc
updated 20 months ago by
xuby963
• 0 • written 4.8 years ago by
truebeliever24
▴ 50
0
votes
3
replies
4.3k
views
psmc bootstrap plotting?
R
genome
software error
updated 4.7 years ago by
morgan
• 0 • written 7.7 years ago by
vulpecula
▴ 30
3
votes
3
replies
1.4k
views
Major issue with DiffBind 3?
atac-seq
diffbind
diffbind3
ChIP-Seq
bioconductor
updated 4.8 years ago by
Rory Stark
★ 2.2k • written 4.8 years ago by
halffedelf
▴ 40
0
votes
0
replies
1.0k
views
qBLAST run and Multiple sequence alignment
XML
alignment
qblast
sequence
updated 2.7 years ago by
Ram
45k • written 5.0 years ago by
gurilion007
• 0
6
votes
9
replies
8.4k
views
regressing out covariate from Seurat integrated data
single-cell
seurat
updated 3.9 years ago by
botloggy
▴ 10 • written 4.8 years ago by
paria
▴ 110
4
votes
2
replies
4.5k
views
How to deal with single nucleus data in Seurat
RNA-Seq
seurat
single nucleus RNA sequencing
updated 4.8 years ago by
Pratik
★ 1.1k • written 5.1 years ago by
bellymountain
▴ 10
1
vote
1
reply
1.1k
views
On read sequencing libraries, the opposite strands are considered on the files? (and how are they handled on assembly?)
reads
sequencing
Assembly
4.8 years ago by
v.berriosfarias
▴ 140
0
votes
3
replies
1.6k
views
How do you create a multiple reference genome in Hisat2?
hisat2
alignment
RNA-Seq
next-gen
assembly
updated 4.8 years ago by
Biostar
20 • written 4.9 years ago by
Aaron
• 0
0
votes
6
replies
2.2k
views
How to modify a BAM file to avoid double-counting of variants from overlapping PE reads?
RNA-Seq
BSseq
4.8 years ago by
lechu
▴ 20
0
votes
0
replies
963
views
Integration or not?
single-cell RNA sequencing
seurat
integration
4.8 years ago by
paria
▴ 110
0
votes
2
replies
888
views
Tumor and matched normal data
wes
wgs
updated 4.8 years ago by
GenoMax
154k • written 4.8 years ago by
shivangi.agarwal800
▴ 120
0
votes
1
reply
2.3k
views
R KEGGREST to query and retrieve specific pathway names for kegg compound ids
keggrest
R
4.8 years ago by
sid5427
▴ 20
0
votes
5
replies
1.3k
views
SNP id from Brainseq and NCBI doesn't match
SNP
ncbi
BrainSeq
database
4.8 years ago by
philosophical.raptor111
• 0
2
votes
1
reply
993
views
Getting sample IDs from dbGaP SRR?
dbgap
updated 4.8 years ago by
Biostar
20 • written 4.9 years ago by
vctrm67
▴ 90
1
vote
0
replies
1.1k
views
Job:
Post-Doctoral Position in Systems Biology & Biomedical Data Sciences (f/m/d)
RNA-Seq
Python
R
updated 2.7 years ago by
Ram
45k • written 4.8 years ago by
a_gruber
▴ 40
2
votes
0
replies
2.0k
views
Job:
PhD Position in Computational Systems Immunology & Data Sciences
R
RNA-Seq
Python
updated 2.7 years ago by
Ram
45k • written 4.8 years ago by
a_gruber
▴ 40
122,217 results • Page
719 of 2445
Recent Votes
Comment: circos plot for genomic features
Answer: How to perform GO enrichment in non-model organisms?
Comment: circos plot for genomic features
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what cause poly-G from NextSeq
what cause poly-G from NextSeq
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Comment: Issue while running Kenddata.
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154k
Look inside the `*.log` files to see if you can get additional clues (and post them here, if you can't figure out things). Check for lines …
Comment: Question about QC and scrublet
by
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3.5k
You can run Scrublet before filtering cells with high gene counts and compare the doublet score vs `n_counts_genes`.
Answer: How to perform GO enrichment in non-model organisms?
by
lieven.sterck
16k
In first instance you will as you say need to assign GOterms to your genes. eggNOG-mapper is certainly a valid approach to do this indeed. …
Comment: circos plot for genomic features
by
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▴ 140
@colindaven thanks a lot! `clinker` also seems to be a nice/effective tool to do so. It happens we stuble across a work where they used `Ci…
Comment: circos plot for genomic features
by
colindaven
8.1k
Why not use something like Jbrowse2 instead ? https://jbrowse.org/jb2/gallery/ You can load both haplotypes, use minimap2 to create a paf …
Comment: How excactly is the Q30 is calculated?
by
colindaven
8.1k
This is really a question for your instrument provider. Only MGI application specialists and their bioinformaticians can really answer this…
Answer: How excactly is the Q30 is calculated?
by
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154k
[**Phred quality scores**][1] have been in use since the 1990s and early days of human genome project. They were co-opted in the fastq form…
Comment: best practice for diploid variant calling
by
Matteo Ungaro
▴ 140
@kevin thanks I was experimenting with the following since I already pursued most of the approaches you mentioned and, in practice, they ar…
Answer: Chip-seq analysis Diffbind
by
ATpoint
90k
I think the results are expected. a) n=2 is underpowered, for any assay and in particular for ChIP-seq which has considerable noise. b) you…
Comment: low quality data or file name swapping -- cellranger arc errors when processing
by
Wu-Sheng Zhang
▴ 10
Hi @arup , after changing the file name following the read length, I can process them using cellranger arc successfully. Thank you very muc…
Comment: Visualize methylation status in Pacbio Hifi read
by
cmdcolin
★ 4.4k
(as the JBrowse dev) I'm glad to hear this. if you see any trouble with it feel free to let me know, I have tried to keep up to date with m…
Comment: low quality data or file name swapping -- cellranger arc errors when processing
by
Wu-Sheng Zhang
▴ 10
Got it! I will try to switch their name and re-run the cellranger arc. Thank you very much, @arup !
Answer: low quality data or file name swapping -- cellranger arc errors when processing
by
Arup Ghosh
3.5k
The barcode files with 24nt read length W71_LUNGrep2_S6_L001_R3_001.fastq.gz and W71_LUNGrep2_S6_L002_R3_001.fastq.gz should be the R2.
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GenoMax
154k
Each database has their own method of annotation/validation. Depending on resources available there may be a lag between the databases in t…
Comment: low quality data or file name swapping -- cellranger arc errors when processing
by
Wu-Sheng Zhang
▴ 10
Hi @arup , thank you very much for your suggestions, and here are the results -- they seems correct. May I have your suggestions? Thank you…
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