Latest
Open
Jobs
Tutorials
Tags
About
FAQ
Community
Planet
New Post
Log In
New Post
Latest
Open
News
Jobs
Tutorials
Forum
Tags
Planet
Users
Log In
Sign Up
About
Limit : all time
all time
today
this week
this month
this year
121,965 results • Page
216 of 2440
Sort: Rank
Rank
Views
Votes
Replies
2
votes
9
replies
2.7k
views
Issues with running featureCounts with STAR
RNA
CLIP-seq
RNA-seq
STAR
updated 2.1 years ago by
pzm
▴ 10 • written 2.2 years ago by
ckim159
• 0
5
votes
3
replies
2.1k
views
homer motif search
motif-search
HOMER
updated 2.1 years ago by
Ram
45k • written 2.1 years ago by
qudrat.nii
▴ 40
4
votes
11
replies
3.5k
views
Trimming of reads in miRNA-Seq data
miRNA-Seq
Trimming
updated 2.1 years ago by
Trivas
★ 1.9k • written 2.1 years ago by
Ezhil La
▴ 40
0
votes
0
replies
639
views
Show mismatches for specific positions in AlignmentsTrack of Gviz package
R
bioconductor
2.1 years ago by
Irsan
★ 7.8k
0
votes
4
replies
1.3k
views
Integrated analysis of RNA-seq datasets
RNA-seq
2.1 years ago by
Petesview
▴ 10
0
votes
2
replies
1.4k
views
GWAS Power Calculation for Quantitative Trait
GWAS
Power
Genetics
updated 2.1 years ago by
Michael
56k • written 4.1 years ago by
Kate
• 0
0
votes
1
reply
814
views
UCSC BLAT miss some matches from hg38
hg38
ucsc
blat
updated 2.1 years ago by
GenoMax
154k • written 2.1 years ago by
Friyunnwoo
▴ 20
0
votes
2
replies
1.5k
views
Confusion about transcript ablation
Ensembl
Variation
VEP
updated 2.1 years ago by
Ben Moore
★ 2.4k • written 2.1 years ago by
Heiha
• 0
0
votes
1
reply
693
views
Annotation of transposons with the EDTA pipeline
EDTA
updated 2.1 years ago by
biofalconch
★ 1.3k • written 2.1 years ago by
xiangjian
• 0
2
votes
7
replies
2.5k
views
VG mapping paired-end reads: error [xg]: multiple hits for XXX
variation-graph
reads
pangenome
vg
paired-end
2.1 years ago by
nkls063408
• 0
0
votes
0
replies
910
views
Forum:
Recruiters: what do you expect on a junior bioinformatician?
career
skills
updated 2.1 years ago by
Ram
45k • written 2.1 years ago by
gallardodiazmiriam
▴ 20
0
votes
2
replies
972
views
Volunteer projects in 2023 for new bioinformaticians
junior
volunteer
projects
2.1 years ago by
gallardodiazmiriam
▴ 20
0
votes
1
reply
1.1k
views
ModBam2BED output from the Epi2Me workflow not being recognized by IGV
methylation
Epi2me
IGV
Nanopore
updated 2.1 years ago by
andres.firrincieli
3.9k • written 2.1 years ago by
Anjan
▴ 850
0
votes
0
replies
785
views
Questions Arising from Using Scanpy for Data Input and scVI for Batch Effect Removal
single
scanpy
cell
scvi
2.1 years ago by
Andy
▴ 120
47
votes
26
replies
6.3k
views
11 follow
Blog:
Evolution of Biostars
meta
Biostars
updated 2.1 years ago by
aldhairmedico
▴ 70 • written 6.6 years ago by
venu
7.1k
5
votes
5
replies
4.6k
views
Error: htsjdk.tribble.TribbleExpection: The provided VCF file is malformed at approximately line number 5880: Duplicate allele added to VariantContex…
SNP
genome
next-gen
Assembly
updated 2.1 years ago by
aldhairmedico
▴ 70 • written 4.7 years ago by
williamsbrian5064
▴ 540
1
vote
2
replies
2.4k
views
htsjdk.tribble.TribbleException: The provided VCF file is malformed
VCF
tribble
GATK
igv
updated 2.1 years ago by
aldhairmedico
▴ 70 • written 3.9 years ago by
Egelbets
▴ 30
1
vote
3
replies
1.2k
views
Theoretical question about scRNA-seq
R
scRNA-seq
updated 2.1 years ago by
dsull
★ 7.7k • written 2.1 years ago by
camillab.
▴ 160
0
votes
0
replies
509
views
Reading frame after aligning DNA for codeml analysis
codeml
reading-frame
dna
alignment
updated 2.1 years ago by
Ram
45k • written 2.1 years ago by
sodiumnitrate
▴ 20
4
votes
4
replies
1.4k
views
Feedback on mouse brain scRNA-seq quality control
mouse
brain
singe-cell
scRNAseq
quality-control
2.1 years ago by
nshenoy
▴ 50
2
votes
4
replies
6.4k
views
Heatmap legend position change
ComplexHeatmap
updated 2.1 years ago by
Ram
45k • written 2.1 years ago by
hellokwmin
• 0
0
votes
1
reply
805
views
RNA-Seq
RNA-Seq
updated 2.1 years ago by
seidel
11k • written 2.1 years ago by
prs
▴ 20
0
votes
1
reply
1.5k
views
Job:
Bioinformatician (Hybrid) @ Tufts University, USA
Bioinformatician
Tufts-University
updated 2.1 years ago by
Ram
45k • written 2.2 years ago by
kyle.monahan
• 0
4
votes
7
replies
1.4k
views
Help with weighted nearest neighbor analysis
seurat
single-cell
2.1 years ago by
Chris
▴ 360
0
votes
0
replies
495
views
similarity of mutation signature matrices
sigprofiler
mutations
denovo-signatures
updated 2.1 years ago by
Ram
45k • written 2.1 years ago by
anubratadas
▴ 20
0
votes
0
replies
530
views
MeRIP analysis: Exomepeak peak calling results are not the same as the IGV shows
m6A
peak-calling
updated 2.1 years ago by
Ram
45k • written 2.1 years ago by
Lu.Lu
• 0
3
votes
2
replies
1.5k
views
reading pgen file into R
pgen
r
snp
updated 2.1 years ago by
Ram
45k • written 2.1 years ago by
Eliza
▴ 30
0
votes
0
replies
484
views
Can HiFi CNV call genotype = 1/1 ?
CNV
HiFi
2.1 years ago by
Nannapat
• 0
0
votes
1
reply
614
views
A tool that performs allele frequency calculations within the Galaxy Platform
galaxy
allele-frequency
updated 2.1 years ago by
Ram
45k • written 2.1 years ago by
LeandroF.
• 0
2
votes
2
replies
1.0k
views
CHIP-Seq data analysis
ChIP-Seq
updated 2.1 years ago by
rfran010
★ 1.6k • written 2.1 years ago by
prs
▴ 20
1
vote
0
replies
566
views
News:
Course - Introduction to CRISPR
CRISPR
Evolution
GenomeEditing
2.1 years ago by
Physalia-courses
★ 2.6k
0
votes
0
replies
770
views
mageckflute scatterview not labeling centric genes
crispr
scatterview
mageckflute
mageck
analysis
2.1 years ago by
buffealo
▴ 130
0
votes
0
replies
573
views
News:
Upcoming Learning Opportunities and Important Updates
R
Programming
aDNA
Paleogenomics
2.1 years ago by
Physalia-courses
★ 2.6k
4
votes
8
replies
2.3k
views
Error executing nf-core/metaboigniter pipeline
nf-core
metaboigniter
nextflow
updated 2.1 years ago by
Phil Ewels
★ 1.5k • written 2.1 years ago by
eesha28112001
• 0
0
votes
0
replies
506
views
Interpretation of Virulence score
WGS
updated 2.1 years ago by
Ram
45k • written 2.1 years ago by
Mustafa
• 0
5
votes
11
replies
3.0k
views
Check Strandedness
Check_Strandedness
how_are_we_stranded_here
leafcutter
bash
updated 23 months ago by
Brian Bushnell
20k • written 2.1 years ago by
Y
▴ 10
0
votes
5
replies
1.5k
views
merge vdj data in citeseq seurat onject
Seurat
updated 2.1 years ago by
Ram
45k • written 2.1 years ago by
kaur
• 0
0
votes
0
replies
1.2k
views
Tutorial:
T Cell Clonal Analysis Using Single-cell RNA Sequencing and Reference Maps
RNAseq
TCR
single-cell
computational
biology
2.1 years ago by
Ming Tommy Tang
★ 4.7k
6
votes
9
replies
2.4k
views
Enricher - Hyper Geometric Test Details
Enricher
ClusterProfiler
DGE
ORA
updated 2.1 years ago by
ATpoint
89k • written 2.1 years ago by
Manuel Sokolov Ravasqueira
▴ 110
4
votes
1
reply
1.6k
views
How to interpret Clustree results?
scRNA
clustering
clustree
updated 2.1 years ago by
LChart
5.1k • written 2.1 years ago by
leranwangcs
▴ 150
3
votes
4
replies
3.5k
views
Forum:
Discussion: Uploading terabytes of data to NCBI SRA
NCBI
WGS
archiving
servers
remote
updated 2.1 years ago by
GenoMax
154k • written 2.1 years ago by
James Reeve
▴ 130
1
vote
1
reply
1.8k
views
Job:
Data Scientist for Bioinformatics and Computer Biology, USA
Statistics
Neuroscience
Data-Scientist
updated 2.1 years ago by
colindaven
8.0k • written 2.1 years ago by
cdrinfo
• 0
0
votes
3
replies
1.2k
views
Limma couldn't find the differential gene
Limma
2.1 years ago by
yoser4
▴ 10
2
votes
5
replies
1.5k
views
6 follow
How to loop over certain files within a directory that belongs to certain samples
shell
fastq
updated 2.1 years ago by
Ram
45k • written 2.1 years ago by
Mohamed Samir
▴ 30
3
votes
4
replies
1.5k
views
simulation of chromosome
snps
simulation
chromosome
2.1 years ago by
Eliza
▴ 30
3
votes
1
reply
735
views
FastQC duplicates questions
FastQC
RNA-seq
2.1 years ago by
Beth
▴ 10
0
votes
2
replies
1.3k
views
BWA-mem2 vs Bowtie2: no deterministic option
bowtie2
bwa
alignment
updated 2.1 years ago by
Ram
45k • written 2.1 years ago by
alessandra.vittorini
• 0
4
votes
9
replies
5.3k
views
7 follow
RVtests CMC output column definitions
SNP
Rvtests
next-gen-sequencing
updated 2.1 years ago by
Ram
45k • written 8.0 years ago by
clyumath
▴ 20
2
votes
3
replies
1.1k
views
blastn - memory leak? Or just obscene usage?
blastn
memory
updated 2.1 years ago by
GenoMax
154k • written 2.1 years ago by
glenn
▴ 10
1
vote
2
replies
966
views
TCGA gene expression quantitation batch information
TCGA
updated 2.0 years ago by
Zhenyu Zhang
★ 1.3k • written 2.1 years ago by
wrab425
▴ 50
121,965 results • Page
216 of 2440
Recent Votes
Answer: How to create a consensus of a contig with samtools or bbmap?
Comment: Getting just fastqc.zip file?
alternate allele frequency and minor allele frequency
Calculating minor allele frequency for GnomAD VCF file
Hiring FT Remote Nextflow engineer to build ML workflows for cancer genomics
Answer: Gene expression equivalent of polygenic risk score ?
A: TRF output to .gff file
Recent Locations •
All
United States,
36 minutes ago
Australia,
1 hour ago
India,
1 hour ago
USA,
2 hours ago
Hong Kong,
2 hours ago
United States,
3 hours ago
Philippines,
3 hours ago
Recent Awards •
All
Popular Question
to
itparanoia
• 0
Popular Question
to
arshad1292
▴ 110
Popular Question
to
marongiu.luigi
▴ 760
Popular Question
to
a615ebfb
▴ 60
Popular Question
to
predeus
★ 2.1k
Popular Question
to
raquel
• 0
Popular Question
to
Jeremy Leipzig
23k
Recent Replies
Comment: How to create a consensus of a contig with samtools or bbmap?
by
marongiu.luigi
▴ 760
sorry, I have mistaken samtools with spades... running `samtools view -h...` did the trick. Thank you.
Comment: Help with Ideathon
by
V K
• 0
Thank you for the response! Unfortunately this is completely independent and not part of a course. I was asking for some innovative ways to…
Answer: How to create a consensus of a contig with samtools or bbmap?
by
lieven.sterck
16k
You assembled a genome using samtools ???? that sounds very weird, if not impossible ... The header (SQ lines) is missing from your file b…
Answer: gnomad par region variants
by
benformatics
4.2k
The XX and XY counts are present on any given variants page.
Comment: Help with Ideathon
by
Mensur Dlakic
★ 30k
I don't see a single question here. Saying `I need your expert help in figuring out how I can make this analysis useful!` is too open-ended…
Comment: Differences between published differential gene expression results and own analy
by
ATpoint
89k
Please link the paper, lets see their methods. With human data it can well be that they included something like surrogate variables to damp…
Comment: Differences between published differential gene expression results and own analy
by
dsull
★ 7.7k
There are many ways to do normalization and one of the correct ways is simply to plug raw counts into deseq2 (the math that deseq2 uses to …
Comment: tximport error (medianLengthOverIsoform)
by
rfran010
★ 1.6k
Is it the version number in your data? e.g. ENST00000415118.1 vs ENST00000415118 could be causing the mismatch?
Comment: Differences between published differential gene expression results and own analy
by
vernonlim98
• 0
So is there any correct way for normalisation? I know limma recommends CPM via limma-voom and DESeq2 just takes in raw counts and does thei…
Comment: Gene expression equivalent of polygenic risk score ?
by
Picasa
▴ 690
Thanks a lot for your answer. I will check the paper.
Comment: Differences between published differential gene expression results and own analy
by
dsull
★ 7.7k
If those logFCs are different, then that's a normalization issue. The logFC is straight forward arithmetic (it's simply dividing mean of […
Comment: Differences between published differential gene expression results and own analy
by
vernonlim98
• 0
Thanks both for your input. It got me to look at the published methodologies more closely, and you guys were right. One paper that I was re…
Comment: Differences between published differential gene expression results and own analy
by
vernonlim98
• 0
Yes it does not match at all, and those genes that are common in both analysis results have very different logFC and p values
Comment: Errors with RSEM/bowtie2
by
Olivia
• 0
I am not sure what you mean by this, but I believe that is what I did. With Trinity, I matched all the paired reads together, so they shoul…
Answer: Gene expression equivalent of polygenic risk score ?
by
GouthamAtla
12k
I don't think something exists out of the box. With variants, we have a 'weight' for each variant on disease risk (obtained through large s…
Traffic: 2832 users visited in the last hour
Content
Search
Users
Tags
Badges
Help
About
FAQ
Access
RSS
API
Stats
Use of this site constitutes acceptance of our
User Agreement and Privacy Policy
.
Powered by the
version 2.3.6