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122,200 results • Page
611 of 2444
Sort: Rank
Rank
Views
Votes
Replies
4
votes
2
replies
2.8k
views
Inserting Gaps into FASTA files for Alignment to Reference
mapping
Alignment
galaxy
FASTA
gap
updated 4.3 years ago by
Istvan Albert
103k • written 4.3 years ago by
lnrrnl
▴ 20
1
vote
2
replies
1.6k
views
Parsing issues with single cell file from GEO
cell
single
parsing
R
updated 4.3 years ago by
Kevin Blighe
★ 90k • written 4.3 years ago by
iddryg
• 0
0
votes
0
replies
1.0k
views
Clarifications about intercepts when fitting models with DESeq2
GLM
rnaseq
DESeq2
DEA
rna-seq
4.3 years ago by
Eisuan
▴ 20
0
votes
1
reply
1.2k
views
using a singualrity application ARGs-OAP
Data-Analysis
WholeShotgunMetagenome
AMR
Microbiome
Metagenomics
updated 4.3 years ago by
ATpoint
90k • written 4.3 years ago by
serene.s
• 0
4
votes
4
replies
3.2k
views
Single-stranded RNA-seq: strandedness of samples
rnaseq
4.3 years ago by
fr
▴ 220
3
votes
4
replies
3.5k
views
Choice of normalization method for spike-in data
spike-in
DiffBind
4.3 years ago by
eashby47
▴ 10
0
votes
1
reply
2.1k
views
Job:
Postdoctoral Position, Department of Biology , Colorado State University
postdoc
updated 2.7 years ago by
Ram
45k • written 4.3 years ago by
Anireddy
• 0
1
vote
6
replies
2.3k
views
How to group transcripts by "gene" from different transcript assemblies?
assembly
trinity
rnaspades
transcript
updated 4.3 years ago by
ponganta
▴ 590 • written 4.3 years ago by
O.rka
▴ 750
0
votes
7
replies
2.5k
views
How to get fold changes from MetaDE package in R?
R
MetaDE
updated 4.3 years ago by
ATpoint
90k • written 4.3 years ago by
humbertojirey
• 0
0
votes
1
reply
993
views
C. elegans WGS large portion of reads flagged as unmapped with Sam flag 133 and 165
sam
WGS
flag
133
165
unmapped
updated 4.3 years ago by
Tm
★ 1.1k • written 4.3 years ago by
tyler.j.kennedy
• 0
0
votes
0
replies
928
views
Help With Cbioportal expression data
rnaseq
TCGA
R
cbioportal
bioconductor
4.3 years ago by
daniela.paola.s.p
▴ 70
2
votes
2
replies
1.2k
views
Pathway Expression Analysis on Individual Cells?
seurat
sc-RNA-seq
4.3 years ago by
ospinae
• 0
0
votes
1
reply
1.1k
views
Protein homolog query issue
transcriptom
blast
species
sequence
Related
updated 4.3 years ago by
Jean-Karim Heriche
27k • written 4.3 years ago by
jaqx008
▴ 110
0
votes
0
replies
623
views
variant impact on immune genes
Genes
Variant
SnpEff
4.3 years ago by
Adarsh Kuamr
▴ 60
0
votes
1
reply
902
views
Protein to gene name conversion
ID
R
updated 4.3 years ago by
GenoMax
154k • written 4.3 years ago by
mm2568
• 0
2
votes
2
replies
965
views
Nanopore dRNA - view unmapped segments of mapped reads
nanopore
sequencing
directRNA
updated 4.3 years ago by
GenoMax
154k • written 4.3 years ago by
yryan
▴ 10
0
votes
0
replies
673
views
What should I write after --operation in ANNOVAR for my interest database ?
ANNOVAR
CIViC
annotation
DoCM
VCF
4.3 years ago by
Zahra
▴ 110
4
votes
7
replies
3.9k
views
Download all Becteria and protist fasta protein sequences from UNIPROT proteomes
uniprot
fetch
fasta
proteome
bash
4.3 years ago by
Chvatil
▴ 140
0
votes
0
replies
759
views
Job:
Bioinformatician (f/m/d)
Hamburg
genomics
Germany
4.3 years ago by
gasta88
▴ 50
0
votes
0
replies
813
views
Job:
Software Engineer / Software Developer (f / m / d) for software in the context of DNA sequencing-based cancer diagnostics
Hamburg
genomics
Germany
4.3 years ago by
gasta88
▴ 50
0
votes
1
reply
812
views
Choosing the right sample among GEO datasets
GEOdatasets
chipsamples
celllinesamples
chipseq
chipseqanalysis
updated 4.3 years ago by
ATpoint
90k • written 4.3 years ago by
buffealo
▴ 130
6
votes
3
replies
6.8k
views
K-means for RNA seq gene clustering
kmeans
updated 4.3 years ago by
Kevin Blighe
★ 90k • written 4.3 years ago by
curiousmind007
▴ 30
3
votes
6
replies
7.1k
views
How do I detect deletions?
bcftools
DNA-seq
calling
variant
updated 4.3 years ago by
bernatgel
★ 3.4k • written 4.3 years ago by
gt
▴ 30
1
vote
3
replies
2.6k
views
Can I use All Peaks (MACS2 -q 1) for analysis?
Peak
DiffBind
MACS2
4.3 years ago by
Tian
▴ 50
0
votes
0
replies
900
views
Job:
UK PhD Opportunity: Text mining the impact of SARS-CoV-2 mutations from the research literature at University of Glasgow
bionlp
sars-cov-2
text-mining
4.3 years ago by
jake.lever
▴ 50
1
vote
4
replies
1.6k
views
How to get from annotated sequences to UniProt IDs
annotation
updated 4.3 years ago by
Tm
★ 1.1k • written 4.3 years ago by
robert.murphy
▴ 110
0
votes
2
replies
1.7k
views
Low read counts in one of three biological replicates. Remove?
RNA-Seq
4.3 years ago by
nadal-t
▴ 20
0
votes
5
replies
2.0k
views
Considering the multiple test correction for the analysis of polygenic risk score association
association
allele
polygenic
score
Bonferroni
updated 4.3 years ago by
German.M.Demidov
★ 3.0k • written 4.3 years ago by
seta
★ 1.9k
0
votes
0
replies
1.7k
views
Job:
Post-doctoral Fellow in Cancer Biology and Immunology
biology
immunology
Cancer
molecular
4.3 years ago by
waihungh
▴ 20
0
votes
0
replies
1.5k
views
Job:
Pacific Biosciences: Senior Bioinformatics Software Engineer (remote)
software-engineer
updated 2.7 years ago by
Ram
45k • written 4.3 years ago by
Armin
• 0
0
votes
1
reply
1.7k
views
annotation parameter in ChIPQC
ChIP-Seq
ChIPQC
updated 4.3 years ago by
384306874
• 0 • written 5.4 years ago by
chaudharyc61
▴ 120
0
votes
0
replies
994
views
Motif finding HOMER results
interpretation
finding
HOMER
motif
4.3 years ago by
c.heininger
▴ 10
5
votes
12
replies
4.0k
views
How do you limit the result from the BLAST executable?
blast
updated 4.3 years ago by
gb
★ 2.2k • written 4.3 years ago by
adhamzul
▴ 20
0
votes
1
reply
925
views
EnsemblVEP could not generate any output for a list of frameshift insertion input
Frame_Shift_Insertion
EnsemblVEP
4.3 years ago by
nazaninhoseinkhan
▴ 530
0
votes
1
reply
946
views
How do I extract predicted genes from annotation from MAKER-P?
MAKER-P
updated 4.3 years ago by
Ram
45k • written 4.3 years ago by
eennadi
▴ 40
0
votes
0
replies
956
views
Renaming ggplot heatmap x-axis from gene names to number of genes
axes
ggplot2
heatmap
4.3 years ago by
Anand
▴ 40
3
votes
1
reply
1.8k
views
genome assembly in org.Mm.eg.db
R
updated 2.7 years ago by
Ram
45k • written 4.3 years ago by
anithaslvn
▴ 10
0
votes
1
reply
1.1k
views
How to find the names of elements while parsing PDB files via biopython?
Biopython
PDB
4.3 years ago by
Tzunami
▴ 10
1
vote
1
reply
1.3k
views
Best current tool for deconvolution of bulk sample
cibersort
updated 4.3 years ago by
Evan
▴ 250 • written 4.3 years ago by
changxu.fan
▴ 80
2
votes
3
replies
1.5k
views
plant viruses sequences
alignment
gene
updated 4.3 years ago by
GenoMax
154k • written 4.3 years ago by
Ric
▴ 440
0
votes
0
replies
896
views
ichorCNA mouse reference files for calling copy number
copynumber
4.3 years ago by
heskett
▴ 110
0
votes
8
replies
1.9k
views
use a list of id to extract sequence from different genomics
sequence
perl
4.3 years ago by
LZH289
• 0
0
votes
0
replies
760
views
Job:
postdoctoral position in bioinformatics/computational proteomics
BionformaticsPostdocUTMB
4.3 years ago by
Rovshan
• 0
0
votes
0
replies
575
views
PoolSNP RuntimeError: dictionary changed size during iteration
Poolsnp
4.3 years ago by
shpak.max
▴ 70
1
vote
1
reply
1.1k
views
What is the right way to merge multiple patient samples in scrna-seq?
Seurat
scrna-seq
cell
processing
updated 4.3 years ago by
ATpoint
90k • written 4.3 years ago by
cogen859
• 0
1
vote
3
replies
1.7k
views
How to filter VEP results of "missing values"
filter
VEP
updated 4.3 years ago by
GenoMax
154k • written 4.3 years ago by
YL
▴ 10
2
votes
2
replies
1.5k
views
Tool:
miRAnno—network-based functional microRNA annotation
pathways
miRNA
annotation
microRNA
4.3 years ago by
tomastokar
▴ 50
0
votes
0
replies
489
views
Determining the effect of dataset size in results
R
4.3 years ago by
a_confused_biologist
• 0
21
votes
14
replies
12k
views
Tool:
trackplot: Fast and minimal dependency standalone R script to generate IGV style locus tracks from bigWig files
visualization
igv
ChIP-Seq
R
bigwigs
updated 2.5 years ago by
Ram
45k • written 5.0 years ago by
poisonAlien
★ 3.2k
1
vote
3
replies
2.2k
views
SSPACE bowtie and bwa error
Assembly
next-gen
software error
genome
updated 4.3 years ago by
hnt001
▴ 10 • written 6.4 years ago by
milady81
▴ 70
122,200 results • Page
611 of 2444
Recent Votes
strong appearing variant not found by haplotypecaller in -ERC mode and deepvariant but with haplotypecaller in normal mode
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Answer: Getting the overlap between two GTF files
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Recent Replies
Comment: low quality data or file name swapping -- cellranger arc errors when processing
by
Wu-Sheng Zhang
• 0
Hi @arup , thank you very much for your suggestions, and here are the results -- they seems correct. May I have your suggestions? Thank you…
Comment: Why did the QV value decrease significantly after using YAHS for HiC scaffolding
by
samuel.a.odonnell
▴ 640
I don't believe merqury ignores softmasked (lower case) nucleotides so I don't think that is the case. From what it sounds like, during th…
Comment: ID unifiying across different datasets
by
zizigolu
★ 4.4k
Thanks a lot to be helpful I’m trying to build a complete `UniProtID` to `GeneSymbol` lookup table and I’m running into a wall. I’ve alrea…
Comment: strong appearing variant not found by haplotypecaller in -ERC mode and deepvaria
by
thomas.heigl.ibk
▴ 20
thanks for the quick reply. i posted the screenshot. gatk-internally, there is still the difference using -ERC or not, priot is getting …
Comment: strong appearing variant not found by haplotypecaller in -ERC mode and deepvaria
by
thomas.heigl.ibk
▴ 20
here the igv view. showing the histogram for all samples plus the reads for one: ![enter image description here][1] and expanded view of …
Comment: low quality data or file name swapping -- cellranger arc errors when processing
by
Arup Ghosh
3.5k
Check the read lengths to make sure the files are correct.
Comment: strong appearing variant not found by haplotypecaller in -ERC mode and deepvaria
by
Pierre Lindenbaum
166k
> Any suggestions or help you could share please, show us an IGV screenshot of the position GATK realign the reads locally, discards read…
Comment: Can i use orthofinder for small protein datasets and not full proteome?
by
alexandrakortsi
• 0
By sequence. Thank you for your response!
Comment: Why did the QV value decrease significantly after using YAHS for HiC scaffolding
by
xinguok794
▴ 10
Thank you for your reply! Unfortunately, despite running YAHS with `--no-contig-ec`, the QV value of the resulting FASTA file did not impro…
Comment: Subsetting before QC in Spatial Transcriptomics
by
Kent
▴ 30
Hi Kevin, Thanks for the detailed explanation. Due to the characteristics of the datasets, we initially used very lenient quality control…
Comment: Midpoint rooting IQTREE newick file moves node support around
by
Luca Arbore
▴ 10
Thank you very much Kevin, it worked!
Comment: ID unifiying across different datasets
by
GenoMax
154k
In this case the entry notes that this is likely the product of a pseudogene: https://www.uniprot.org/uniprotkb/Q5VTE0/entry and existence …
Comment: Comparison of different RNAseq data sets
by
DrSmad
▴ 10
Each lab contributes both control and LPS. Example, for cell line A_lab1 did and analysis on control and LPS-6h. Cell line B_lab2 did contr…
Comment: ID unifiying across different datasets
by
zizigolu
★ 4.4k
sorry, why some gene names are often lacking though the Uniprot ID is still valid (using biomart)?
Comment: snpEff: Unsupported structural variant types
by
shpak.max
▴ 70
Unfortunately, while it ran without a problem initially, when I checked the run screen today, I saw the following error message (and unlike…
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