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121,963 results • Page
204 of 2440
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Rank
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Votes
Replies
2
votes
4
replies
2.1k
views
Using STAR aligner to build index of hg38
hg38
STAR
alignment
RNAseq
index
2.0 years ago by
Grace
• 0
0
votes
2
replies
910
views
Modify the code to take most abundant reads from a cluster and process it.
cd-hit-est
clustering
2.0 years ago by
Mo
▴ 50
1
vote
2
replies
881
views
Understanding TCGA barcodes with dot in the fieldname
tcga
updated 2.0 years ago by
Zhenyu Zhang
★ 1.3k • written 2.0 years ago by
Tahsin
• 0
0
votes
0
replies
498
views
Compare peaks between clusters in sc-ATAC
Peak-Calling
Epigenome
scATAC-seq
updated 2.0 years ago by
Ram
45k • written 2.0 years ago by
Ahmed.waraky
▴ 10
1
vote
3
replies
1.4k
views
How to DESeq2 using miRNA data obtained using TCGAbiolinks
R
TCGAbiolinks
DESeq2
TCGA
updated 2.0 years ago by
Zhenyu Zhang
★ 1.3k • written 2.0 years ago by
Mo
• 0
0
votes
8
replies
3.2k
views
6 follow
Highly inflated p-values in GWAS by regenie
regenie
plink
gwas
updated 4 months ago by
zx8754
12k • written 2.0 years ago by
cwwong13
▴ 40
1
vote
3
replies
1.3k
views
How to find out what adapters to remove after FastQC of RNAseq data?
Trimmomatic
FastQC
NGS
RNA-seq
2.0 years ago by
ella
• 0
2
votes
5
replies
2.7k
views
Trimmomatic .jar not included anymore?
trimmomatic
ubuntu
linux
updated 2.0 years ago by
petebio
▴ 100 • written 2.0 years ago by
Emily
▴ 70
0
votes
1
reply
1.1k
views
News:
EMBL-EBI virtual course | Introduction to RNA-seq and functional interpretation
RNA-seq
updated 2.0 years ago by
Ram
45k • written 2.0 years ago by
Rebecca
• 0
2
votes
7
replies
2.3k
views
Weirdness in annotation (missing allele frequencies)
allele-frequency
gnomad
annovar
updated 2.0 years ago by
Ram
45k • written 2.0 years ago by
Can Abdullah
• 0
0
votes
1
reply
1.1k
views
High amount of intronic/intergenic reads in SMARTer stranded total bulk RNAseq
RNA-seq
DNA
SMARTer
updated 2.0 years ago by
Ram
45k • written 2.0 years ago by
Mat
▴ 80
3
votes
7
replies
2.1k
views
How to check RNAseq support for annotated genes?
gene
RNA-seq
annotation
updated 2.0 years ago by
Michael
56k • written 2.0 years ago by
BioinfoBee
• 0
0
votes
0
replies
771
views
Why dbConnect GEOmetadb_demo.sqlite shows some information while dbConnect GEOmetadb.sqlite shows no information
R
GEO
GEOmetadb
updated 2.0 years ago by
Pierre Lindenbaum
166k • written 2.0 years ago by
nonaddldy
▴ 10
1
vote
0
replies
877
views
News:
Online Training - Bioinformatics Pipeline Development with Nextflow (November 15-17, 2023)
nextflow
automation
pipeline
development
2.0 years ago by
David Langenberger
11k
2
votes
5
replies
1.8k
views
ATAC-seq troubleshoot - Just Noise
ATAC-seq
updated 2.0 years ago by
ATpoint
89k • written 2.0 years ago by
vk
▴ 40
2
votes
2
replies
1.2k
views
Simulate short-read RNA-seq data from long-read RNA-seq data
polyester
single-cell
simulation
short-read
long-read
2.0 years ago by
rhonddaskl
• 0
4
votes
4
replies
1.8k
views
DESeq2 analysis using two featureCounts generated from different studies
RNA-seq
DESeq2
2.0 years ago by
abedkurdi10
▴ 190
4
votes
4
replies
1.5k
views
Filtering VCF to divide with equal sizes
bcftools
vcf
updated 2.0 years ago by
Ram
45k • written 2.0 years ago by
avelarbio46
▴ 30
0
votes
0
replies
628
views
High pvalues when using clusterProfiler for seurat
clusterProfiler
2.0 years ago by
Ahmed
▴ 10
6
votes
3
replies
1.6k
views
kallisto normalized TPM values without bootstraps
tpm
cibersort
sleuth
kallisto
RNA-seq
updated 13 months ago by
binbinZhao
• 0 • written 2.0 years ago by
butterman16
▴ 30
5
votes
7
replies
2.0k
views
Salmon index not progressing
salmon
updated 2.0 years ago by
Michael
56k • written 2.0 years ago by
camillab.
▴ 160
0
votes
0
replies
1.2k
views
scanpy problem for empty cells
scanpy
updated 2.0 years ago by
Ram
45k • written 2.0 years ago by
Andy
▴ 120
0
votes
0
replies
596
views
Current landscape of approaches to scRNA-seq with nanopore sequencers?
scRNA-seq
nanopore
single-cell
2.0 years ago by
LauferVA
4.8k
0
votes
1
reply
1.2k
views
How to download genomes and proteins from JGI in bulk via the command line?
jgi
cli
updated 2.0 years ago by
Ram
45k • written 2.0 years ago by
O.rka
▴ 750
2
votes
1
reply
935
views
News:
Successful NCBI NIAID Codeathon on VCF Files in SARS-CoV-2 Genomics
NCBI
Codeathon
updated 2.0 years ago by
chrchang523
11k • written 2.0 years ago by
PeterC_NCBI
▴ 520
3
votes
4
replies
1.4k
views
Chromosome bias on RNA-Seq differential gene expression analysis
chromosome-bias
RNA-seq
2.0 years ago by
blz
▴ 40
6
votes
2
replies
1.5k
views
Identifying common DEGs among multiple datasets
R
DEG
updated 2.0 years ago by
Barry Digby
★ 1.3k • written 2.0 years ago by
Shma
▴ 20
3
votes
3
replies
2.1k
views
Forum:
Importance of Data Structures for Bioinformatics?
data-structures
updated 2.0 years ago by
Ram
45k • written 2.0 years ago by
S
• 0
0
votes
2
replies
974
views
How to find positions with higher depth relative to their surroundings
depth
python
samtools
updated 2.0 years ago by
xiaoguang
▴ 160 • written 2.0 years ago by
hyperdx1
• 0
0
votes
0
replies
650
views
News:
Research Breakthrough in Identifying Viral Escape Mutations for Improved Therapeutic Design
sequence-analysis
sars-cov-2
spike-protein
updated 2.0 years ago by
Ram
45k • written 2.0 years ago by
Prem
• 0
3
votes
2
replies
1.1k
views
How to retrieve LoF and missense variants in WES data?
bcftools
variants
plink
SNPs
updated 2.0 years ago by
luffy
▴ 130 • written 2.0 years ago by
_quantum_girl_
▴ 60
0
votes
0
replies
793
views
Recommended workflow for identifying the genomic location and copy-number of an insert with a known sequence from WGS Nanopore fastq files
Nanopore
WGS
Long-Read
updated 2.0 years ago by
Ram
45k • written 2.0 years ago by
dk0319
▴ 70
4
votes
0
replies
996
views
Herald:
The Biostar Herald for Wednesday, September 20, 2023
herald
2.0 years ago by
Biostar
3.6k
1
vote
4
replies
1.2k
views
I need to retrieve a set of protein and mRNA sequences
Protein
mRNA
sequences
updated 2.0 years ago by
Ram
45k • written 2.0 years ago by
george
• 0
0
votes
1
reply
1.1k
views
Esearch, Epost, and Efetch for Large Datasets in Biopython
eutils
biopython
entrez
updated 2.0 years ago by
Ram
45k • written 2.0 years ago by
Salem
• 0
1
vote
2
replies
1.5k
views
GSEA Result Visualization in R
r
enrichplot
gsea
visualization
enrichResult
2.0 years ago by
Cortney
• 0
1
vote
2
replies
1.2k
views
How to separate proteins on the same chain?
pdb
protein
updated 2.0 years ago by
Ram
45k • written 2.0 years ago by
Zayyan
▴ 10
0
votes
2
replies
1.0k
views
how to evaluate SNPs that are regulating same gene expression across multiple tissues
snp
GTEx
updated 2.0 years ago by
LChart
5.1k • written 2.0 years ago by
rheab1230
▴ 150
3
votes
10
replies
2.6k
views
STAR index not working
STAR
RNA-Seq
2.0 years ago by
camillab.
▴ 160
1
vote
2
replies
2.0k
views
How to display all top markers in the heatmap by DoHeatmap (Seurat) when there are duplicates of top marker genes for several cell clusters
DoHeatmap
Seurat
2.0 years ago by
alwayshope
▴ 40
2
votes
3
replies
1.4k
views
Can I infer the fraction of replicating cells from bulk RNA-seq data?
replication
apoptosis
updated 2.0 years ago by
Ram
45k • written 2.0 years ago by
txema.heredia
▴ 250
0
votes
1
reply
627
views
Prank checkpoint and restore?
prank
alignment
updated 2.0 years ago by
Ram
45k • written 2.0 years ago by
Pit
• 0
0
votes
0
replies
3.0k
views
Job:
Research Scientist 5 – Bioinformatics and Computer Biology, Center for Dementia Research (CDR), Nathan Kline Institute for Psychiatric Research
Neuroscience
Biostatistics
updated 2.0 years ago by
Ram
45k • written 2.0 years ago by
cdrinfo
• 0
1
vote
1
reply
1.3k
views
gffread outputs empty gtf file
gff
gffread
gtf
updated 2.0 years ago by
inedraylig
▴ 70 • written 2.0 years ago by
sumitra.20
• 0
0
votes
13
replies
2.2k
views
STAR Intron Motif Script Gives Segmentation fault Error
STAR
Linux
2.0 years ago by
Y
▴ 10
5
votes
7
replies
2.6k
views
Elusive syntax error in Snakefile
snakemake
updated 2.0 years ago by
Ram
45k • written 2.0 years ago by
Giuseppe Giovanni
▴ 30
1
vote
3
replies
1.1k
views
Sub-sampleing bam files based on sequencing_summary.txt (guppy output)
samtools
guppy
updated 2.0 years ago by
GenoMax
154k • written 2.0 years ago by
aj
• 0
8
votes
10
replies
3.2k
views
Inflated GWAS test statistic after merging multiple batches of genotype dataset imputed differently
genotype
imputation
gwas
updated 2.0 years ago by
LauferVA
4.8k • written 2.0 years ago by
Amy
▴ 20
0
votes
13
replies
2.6k
views
Dealing with transcriptome sequences that are smaller than their respective genes
blastn
Trinity
Transcriptome
De-novo-transcriptome-assembly
RNA-seq
updated 24 months ago by
Ram
45k • written 2.0 years ago by
langziv
▴ 70
2
votes
2
replies
1.9k
views
Kraken2 recovering only classified reads
Kraken2
taxonomy
classification
2.0 years ago by
SushiRoll
▴ 140
121,963 results • Page
204 of 2440
Recent Votes
Answer: Gene expression equivalent of polygenic risk score ?
A: TRF output to .gff file
A: GATK ASEReadCounter: Downstream analysis for identifying allele specific express
Comment: Differences between published differential gene expression results and own analy
A: Which is the proper RNA-seq count table transformation to perform hierarchial cl
Answer: Differences between published differential gene expression results and own analy
Answer: If TPM is not comparable across cohorts, can it be used as the input for ML mode
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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…
Comment: ESTIMATE (Estimation of STromal and Immune cells in MAlignant Tumor tissues usin
by
Ben
• 0
write.table(df1, "df1.txt", sep = "\t", row.names = T, col.names = T, quote = FALSE)
Comment: Errors with RSEM/bowtie2
by
GenoMax
154k
That is good confirmation. Bacl to the error message. > I don't know how to fix this, given that I already did the trimming steps. DId yo…
Comment: Differences between published differential gene expression results and own analy
by
dsull
★ 7.7k
Honestly, those things shouldn't result in a considerable discrepancy. The largest difference will come from the post-processing & analysi…
Answer: Differences between published differential gene expression results and own analy
by
Ales
▴ 50
I second the comment about comparing the top 100 genes - if you see vastly different results, I would lean closer to examining protocols th…
Answer: Help interpreting BLASTn results and phylogenetic tree for genetics practical
by
Mensur Dlakic
★ 30k
I think what you are asking involves too much work for anyone to explain it in granular detail. But who knows, maybe there is a good soul o…
Answer: Differences between published differential gene expression results and own analy
by
yura.grabovska
▴ 830
When you say vastly different, what do you mean exactly? Does your top 100 up/down not match theirs at all?
Comment: Functional prediction for proteins of bacteria.
by
colindaven
8.0k
Have a look at tools like SnpEff or Ensembl VEP. Perhaps your bacterial sp is included.
Comment: Errors with RSEM/bowtie2
by
Olivia
• 0
Yes, I already made the transcriptome with these tools, and the CD-HIT-EST fasta file is the transcript file that I am using for RSEM. Then…
Comment: sra-explorer : find SRA and FastQ download URLs in a couple of clicks
by
Guilherme
• 0
Oh, ok. It seems like NCBI stores the files in SRA format (thus needing conversion and database lookups by sra toolkit tools) and EBI store…
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