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121,845 results • Page
406 of 2437
Sort: Rank
Rank
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Votes
Replies
1
vote
4
replies
2.7k
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GenotypeGVCF too many genotypes from pooled samples
GenotypeGVCFs
GATK
VCF
updated 15 months ago by
Sd
• 0 • written 4.3 years ago by
Vic
▴ 130
0
votes
6
replies
1.6k
views
Feedback on Workflow
WGS
pipeline
3.2 years ago by
01de
▴ 10
0
votes
1
reply
790
views
Indel size seemingly capped by software?
indels
calling
nucmer
variant
genome
alignment
3.2 years ago by
mrmrwinter
▴ 30
5
votes
4
replies
1.2k
views
DESEQ2 study design for different time points between controls and high dose samples.
drug
DEGs
DESEQ2
exposure
updated 3.2 years ago by
Basti
★ 2.1k • written 3.2 years ago by
salman_96
▴ 70
0
votes
1
reply
805
views
high frequency subsequences
biopython
FASTA
updated 2.2 years ago by
Ram
45k • written 3.2 years ago by
setschmann
▴ 10
0
votes
0
replies
471
views
Rankprod
gene
differential
expression
analysis
Rankprod
3.2 years ago by
nishimalhotra2612
▴ 50
6
votes
5
replies
2.4k
views
UniProt REST Mapping Problem
UniProt
mapping
Python
REST
Ensembl
3.2 years ago by
ngarber
▴ 60
0
votes
0
replies
465
views
Obtain FREQ column for a summary statistics
Statistic
Summary
Freq
MAF
3.2 years ago by
Mahan
▴ 70
0
votes
1
reply
1.8k
views
qp3pop missing pop error?
q3Pop
Admixtools
f3test
updated 3.2 years ago by
francesco.fontani2
• 0 • written 5.1 years ago by
sam980406
• 0
0
votes
1
reply
2.6k
views
Understanding ABI Sanger File Format
Sequencing
Sanger
Python
ABI
updated 3.2 years ago by
trausch
★ 2.0k • written 3.2 years ago by
oludhe
▴ 90
0
votes
1
reply
817
views
bedgraphToBigWig error
Bedgraph
ucscPath
BigWig
R
updated 3.2 years ago by
GenoMax
153k • written 3.2 years ago by
Mireia
• 0
0
votes
0
replies
599
views
How can I understand aggregate in FAN-C tool using Hi-C data?
Hi-C
TAD
FAN-C
aggregate
fanc
3.2 years ago by
woongjaej
▴ 30
8
votes
3
replies
1.7k
views
Bulk RNA-seq with genome but without gene annotation
GFT
wouthou
analysisz
RNA-seq
updated 3.2 years ago by
colindaven
7.8k • written 3.2 years ago by
Diego
▴ 110
1
vote
0
replies
654
views
News:
Data analysis with the Tidyverse in July (18th-21st).
Visualization
R
Tidyverse
data-analysis
updated 3.2 years ago by
Ram
45k • written 3.2 years ago by
Physalia-courses
★ 2.6k
0
votes
8
replies
3.4k
views
could not find function "pickSoftThreshold"
R
updated 2.3 years ago by
Ram
45k • written 3.2 years ago by
Sonia
• 0
0
votes
2
replies
1.6k
views
Pearson correlation matrix heat map. The different colors represent Pearson correlation coefficients, and the diverse circle sizes represent P value.
bubble
R
plot
correlation
updated 3.2 years ago by
Asaf
10k • written 3.2 years ago by
Fahmida Khanam
• 0
1
vote
2
replies
789
views
Multiple copies of same gene annotated
CDS
Gene
Prokka
3.2 years ago by
SK007
• 0
2
votes
1
reply
1.2k
views
how can i fix this problem in R
DESeq2
S4Vectors
updated 3.2 years ago by
cpad0112
21k • written 3.2 years ago by
Habib
• 0
0
votes
0
replies
484
views
Output dosage file by PLINK or other software
pgen
bed
plink
dosage
output
3.2 years ago by
Roxy
• 0
1
vote
2
replies
2.4k
views
bowtie2 error "Unable to read file magic number"
fastq
Bowtie2
updated 3.2 years ago by
ATpoint
89k • written 3.2 years ago by
rottenwasabi
• 0
0
votes
1
reply
840
views
david ID conversion
tag
conversion
locus
ID
david
updated 3.2 years ago by
GenoMax
153k • written 3.2 years ago by
hana
• 0
0
votes
0
replies
545
views
Bio.motifs.threshold module
PSSM
Bio.motif
3.2 years ago by
nyanovsky
• 0
1
vote
1
reply
834
views
What is an acceptable pairwise alignment % for a MSA
MSA
MUSCLE
updated 3.2 years ago by
Mensur Dlakic
★ 29k • written 3.2 years ago by
aframirez
• 0
0
votes
0
replies
438
views
WGS based variant analysis for biomarkers
WGS
sequencing
statistics
3.2 years ago by
halo22
▴ 300
2
votes
2
replies
1.3k
views
Use of Scater for QC in scRNA-seq Analysis: How to remove cells with less than certain number of genes supported with certain number of reads
SingleCellExperiment
3.2 years ago by
otieno43
▴ 40
0
votes
1
reply
698
views
Find motif position given a set of enrich peaks
peaks
position
Motif
updated 3.2 years ago by
tobiaminuxy
• 0 • written 3.2 years ago by
Abdelhamid
• 0
0
votes
3
replies
1.4k
views
No module named 'msprime'
module
python
msprime
no
vscode
3.2 years ago by
desptsp
• 0
0
votes
1
reply
740
views
Intergenic distance
gff
gene
updated 2.7 years ago by
Ram
45k • written 3.2 years ago by
h_asma
• 0
0
votes
0
replies
423
views
Find motifs close to nanog motifs from Fimo output
fimo
3.2 years ago by
tobiaminuxy
• 0
0
votes
1
reply
681
views
How can I transform a three column data frame into a binary-table in R?
rstudio
updated 3.2 years ago by
brunobsouzaa
▴ 840 • written 3.2 years ago by
Camilo Andres
▴ 40
0
votes
4
replies
1.1k
views
[R] Differential Co-Expression ?
R
edgeR
GEO
3.2 years ago by
ali
▴ 20
2
votes
2
replies
1.0k
views
It is weird there are no reads less than 100 bp in qualimap.
qualimap
3.2 years ago by
Dan
▴ 180
0
votes
0
replies
291
views
What is the differences between using Shared Sequence Variants and OTUs?
genomics
3.2 years ago by
Phú
• 0
0
votes
0
replies
500
views
Differential expression with single cell data: any good two component (hurdle) models after MAST?
RNA-Seq
single-cell
MAST
next-gen-sequencing
updated 3.2 years ago by
Ram
45k • written 3.2 years ago by
ntuzov
• 0
0
votes
1
reply
1.5k
views
Job:
Need a RNASeq Analysis tutor
rnaseq
tutor
analysis
differential
updated 3.2 years ago by
Mensur Dlakic
★ 29k • written 3.2 years ago by
smithkthedale
▴ 10
0
votes
0
replies
678
views
[R] Extract Normalized Counts from DGEList (edgeR) ?
R
edgeR
GEO
3.2 years ago by
ali
▴ 20
0
votes
0
replies
415
views
MERLIN haplotyping
MERLIN
3.2 years ago by
smb2174
▴ 20
0
votes
0
replies
576
views
STR expansion detection on IonTorrent WES data?
repeat
STR
IonTorrent
wes
ngs
short
tandem
3.2 years ago by
Joel Wallenius
▴ 220
0
votes
0
replies
669
views
What is the significance of "Zero Cross" in Ranked List Metric in Gene Set Enrichment Analysis ?
GSEA
GeneSetEnrichment
3.2 years ago by
bnayer26
• 0
0
votes
0
replies
512
views
which genome size to use in Fisher's exact test for enrichment?
Fisher
enrichment
3.2 years ago by
druggable
▴ 60
2
votes
4
replies
1.2k
views
how to extract columns from csv using a list of name
R
excel
updated 3.2 years ago by
Basti
★ 2.1k • written 3.2 years ago by
baijiangshan9726
• 0
0
votes
1
reply
1.3k
views
Job:
Staff Scientist - Bioinformatician, Baylor College of Medicine, Human Genome Sequencing Center, Houston, United States
NGS
TGS
updated 2.2 years ago by
Ram
45k • written 3.2 years ago by
Medhat
9.8k
3
votes
0
replies
904
views
Herald:
The Biostar Herald for Tuesday, June 28, 2022
herald
3.2 years ago by
Biostar
3.6k
0
votes
0
replies
515
views
How to convert CEL file to PLINK format
snp
vcf
plink
apple
cel
3.2 years ago by
Mira
• 0
1
vote
2
replies
1.0k
views
VCF file format | Mandatory information
VCF
fields
Mandatory
updated 3.2 years ago by
GenoMax
153k • written 3.2 years ago by
its.roops
• 0
0
votes
0
replies
500
views
Gene classification
gene
classification
3.2 years ago by
biology_inform
▴ 60
4
votes
3
replies
1.5k
views
why bowtie2 doesn’t report longer than 500bp inserts?
bowtie2
BAM
updated 3.2 years ago by
acvill
▴ 350 • written 3.2 years ago by
Dan
▴ 180
0
votes
2
replies
832
views
Efficiently detect Structural Variant
variant
Structural
3.2 years ago by
its.roops
• 0
6
votes
3
replies
1.3k
views
[R] Same Analysis but different results ?
R
edgeR
GEO
updated 3.2 years ago by
Giovanni M Dall'Olio
28k • written 3.2 years ago by
ali
▴ 20
5
votes
1
reply
821
views
Using gtf file to get gene positions
gtf
sequencing
R
igv
updated 2.7 years ago by
Ram
45k • written 3.2 years ago by
margo
▴ 40
121,845 results • Page
406 of 2437
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Answer: DESeq2 time-series - full model matrix is less than full rank
Answer: DESeq2 time-series - full model matrix is less than full rank
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Answer: RNAseq requirements: Biological and Technical replicates
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Recent Replies
Answer: ATAC-seq fragment size distribution - huge spike at 150 bp
by
yuntan1992
• 0
After removing adapters with trim_galore, change the parameter of bowtie2 " --local" to "--end-to-end".
Comment: Tools for raw reads that estimate the percentage of reads that hit marker genes
by
shevch2009
▴ 20
That is a great comparison! :) It definitely looks that way. :) It's not about taxonomy, but about reconstructing metabolic pathways direc…
Comment: How to connect the UCSC when i get the DMR.plot?
by
Wren
• 0
I tried using the main site but it still didn't work. Thanks anyway, I'll try other methods.
Answer: Tools for raw reads that estimate the percentage of reads that hit marker genes
by
Mensur Dlakic
★ 29k
If you want an overall taxonomic profile, this tool will do it from reads directly: https://github.com/DessimozLab/read2tree > Well, …
Answer: Tools for raw reads that estimate the percentage of reads that hit marker genes
by
LChart
5.0k
I have used BURST (https://github.com/knights-lab/BURST) to do this before. You can take fastA sequences for your target genes and build ou…
Comment: RNAseq requirements: Biological and Technical replicates
by
Ram
45k
Why not just say "technical replicates are necessary"?
Comment: Tools for raw reads that estimate the percentage of reads that hit marker genes
by
shevch2009
▴ 20
Well, we already have mags, but my boss want to check the raw reads, that is why I am trying to find a way. Well, human got me errors, it…
Comment: Tools for raw reads that estimate the percentage of reads that hit marker genes
by
GenoMax
153k
Then you need to decide if you want to assemble your reads into contigs/MAG's followed by using the tools discussed. Or do the mapping usin…
Comment: Tools for raw reads that estimate the percentage of reads that hit marker genes
by
shevch2009
▴ 20
I considered mapping the reads to a database, but that approach wouldn't provide the gene names or the metabolic pathways the genes partici…
Comment: Criteria for choosing variants
by
ramiro.barrantes
▴ 60
Thank you. It has not been my understanding or experience that calling variants in tumor-normal pairs is straightforward, especially somati…
Comment: Tools for raw reads that estimate the percentage of reads that hit marker genes
by
shevch2009
▴ 20
I don't think any kind of web-based tool will work; the read files are very large (at least 10 GB). Usually, web versions have restrictions…
Comment: Tools for raw reads that estimate the percentage of reads that hit marker genes
by
GenoMax
153k
A quick look suggests that this tool is expecting longer sequences (if the example is to go by in sequence search) that need to be protein …
Answer: Tools for raw reads that estimate the percentage of reads that hit marker genes
by
colindaven
7.8k
I believe **Mgnify** at the EBI https://www.ebi.ac.uk/metagenomics does something like this for you using domains. But I have not used it, …
Comment: Low Mapping Rate with Kallisto on RNA-seq Data
by
GenoMax
153k
> I checked for contamination using fastq_screen, and most of the reads (>90%) mapped to human genome on a subset of 2M reads. Looks like …
Comment: Low Mapping Rate with Kallisto on RNA-seq Data
by
Buffo
★ 2.4k
Kallisto is a pseudoaligner, so, as @atpoint suggested, it could be DNA contamination. You can confirm this using an aligner and a referenc…
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