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121,844 results • Page
407 of 2437
Sort: Rank
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Votes
Replies
0
votes
0
replies
448
views
Bimodal read lenghts in pacbio transcriptome sequencing
libraries
pacbio
rna-seq
transcriptome
3.2 years ago by
Carlos
• 0
0
votes
5
replies
1.5k
views
Which miRNA arm to select for target prediction, 3p or 5p?
Target-Prediction
miRNA
DESeq2
updated 2.7 years ago by
Ram
45k • written 3.2 years ago by
Tusharika
• 0
2
votes
8
replies
3.1k
views
Quick download of FASTQ
aspera
sratoolkit
fastq
updated 3.2 years ago by
ATpoint
89k • written 3.2 years ago by
Thanh
• 0
1
vote
2
replies
860
views
Less reads are shown using sample_sums() through phyloseq
vegan
Phyloseq
and
3.2 years ago by
梓明
▴ 10
0
votes
2
replies
1.1k
views
Bacterial contamination in human DNA sample
Long-read-sequencing
Bacterial-contamination
updated 17 months ago by
Ram
45k • written 3.2 years ago by
priya.bmg
▴ 70
0
votes
0
replies
386
views
Linear alignment
alignment
mapping
updated 2.7 years ago by
Ram
45k • written 3.2 years ago by
Shaima
• 0
3
votes
3
replies
1.8k
views
Extract first and last column of fasta-header
sequence
updated 3.2 years ago by
Hugo
▴ 400 • written 3.2 years ago by
genomes_and_MGEs
▴ 10
0
votes
1
reply
588
views
RNAseq analysis: I have read counts for all CDS. Could I use standard methods (limma-voom, edgeR) for DEA??
RNAseq
DGE
CDS
mapping
DEA
updated 3.2 years ago by
ATpoint
89k • written 3.2 years ago by
Elena
• 0
0
votes
0
replies
506
views
the pos in sam file generated by minimap2 can not be correctly parsed.
CIGAR
minimap2
pos
3.2 years ago by
Aaron
▴ 10
2
votes
2
replies
1.1k
views
cram to fastq
cram
fastq
updated 3.2 years ago by
ATpoint
89k • written 3.2 years ago by
junnna
▴ 10
2
votes
1
reply
1.7k
views
Converting GP field in a VCF to GT
VCF
Threshold
GT
GP
3.2 years ago by
Garan
▴ 700
1
vote
0
replies
766
views
News:
Use your standard DNA variant caller for SNP calling in Bisulfite-Seq data
bisulfite
BS-Seq
methylation
3.2 years ago by
David Langenberger
11k
1
vote
1
reply
801
views
volcano plot display selected labels
volcanoplot
enhancedvolcano
rna-seq
updated 3.2 years ago by
Kevin Blighe
89k • written 3.2 years ago by
biology_inform
▴ 60
1
vote
3
replies
997
views
R can install .zip package but not .tar.gz package
R
updated 3.2 years ago by
Basti
★ 2.1k • written 3.2 years ago by
Nickier
▴ 20
0
votes
0
replies
501
views
Variant calling from merged bam file with one vcf output
bam
WGS
variant
calling
3.2 years ago by
askif4
▴ 20
1
vote
2
replies
1.0k
views
Match genes with the pathway they participate
genes
pathways
databases
updated 3.2 years ago by
cpad0112
21k • written 3.2 years ago by
eleni.psar
• 0
0
votes
0
replies
648
views
Blog:
Using Transcriptome Sequencing to identify DEGs in response to chemical challenges
Sequencing
RNAseq
Transcriptome
NGS
3.2 years ago by
Novogene
▴ 510
1
vote
10
replies
6.9k
views
How to ensure all fonts are written in Arial for EnhancedVolcano?
EnhancedVolcano
22 months ago by
junli1988
• 0
0
votes
0
replies
546
views
Difference between query_alignment_length, template_length, reference_length
pysam
3.2 years ago by
tien
▴ 40
0
votes
0
replies
584
views
How to add to a VCF file's sample information into INFO column?
VCF
R
updated 2.2 years ago by
Ram
45k • written 3.2 years ago by
wrinklypalms
• 0
2
votes
1
reply
769
views
Why does the CADD database have multiple lines for the same mutation/substitution with different gene IDs?
cadd
updated 3.2 years ago by
tomas4482
▴ 430 • written 3.2 years ago by
4galaxy77
2.9k
1
vote
3
replies
1.4k
views
How to find DEG within a cluster between two groups without any replication information in scRNA-Seq analysis?
scRNA-Seq
Seurat
Pseudobulk
updated 3.2 years ago by
piyushjo
▴ 710 • written 3.2 years ago by
Zahra
▴ 110
0
votes
1
reply
715
views
Check if sequence is cytosol-facing?
Topology
Protein
Python
Motif
updated 3.2 years ago by
Mensur Dlakic
★ 29k • written 3.2 years ago by
ngarber
▴ 60
0
votes
0
replies
624
views
Replicated samples analysis
repeats
replicates
3.2 years ago by
valentinavan
▴ 50
0
votes
0
replies
1.3k
views
Job:
Research Software Engineer, Department of Data Science, Dana-Farber Cancer Institute
engineer
software
3.2 years ago by
Laura
• 0
0
votes
1
reply
835
views
How can I parse alternative atom information in a PDB file?
pdb
protein
updated 3.2 years ago by
Wayne
★ 2.1k • written 3.2 years ago by
user366312
▴ 20
0
votes
7
replies
1.8k
views
can not find certain genes: Ensembl_Gene_Id To Entrezgene using Biomart
gene
R
Biomart
ID
updated 3.2 years ago by
GenoMax
153k • written 3.2 years ago by
catherine
▴ 250
1
vote
4
replies
2.5k
views
Plink: .vcf to .ped issue (problem with polyploidy?)
polyploidy
ped
Plink
updated 2.5 years ago by
Ram
45k • written 3.4 years ago by
Alice
• 0
1
vote
2
replies
963
views
mRNA contamination in miRNA prep
RIN
miRNA
3.2 years ago by
Abhishek
• 0
0
votes
1
reply
692
views
DTU by combining different type of RNA seq data
DTU
analysis
updated 3.2 years ago by
Trivas
★ 1.9k • written 3.2 years ago by
aimanbarki
▴ 20
1
vote
1
reply
866
views
Where to find terra (telomeric RNA) coordinates?
rnaseq
Alignment
mapping
updated 3.2 years ago by
Giovanni M Dall'Olio
28k • written 3.2 years ago by
PK
▴ 130
0
votes
0
replies
595
views
Allelic fraction from WES data
Fraction
VAF
Whole-exome
sequencing
Allelic
3.2 years ago by
Hasib
▴ 20
1
vote
4
replies
2.2k
views
How to compare two sequence logo?
sequence-logo
motif
updated 3.2 years ago by
Ram
45k • written 3.2 years ago by
Andrew Liu
▴ 10
0
votes
0
replies
957
views
MACS2: broad and broad no-model output peaks are exactly the same. Is something wrong?
ChIP-seq
macs2
H3K27ac
3.2 years ago by
piyushjo
▴ 710
1
vote
3
replies
1.0k
views
Finding a known duplication mutation in a VCF file
vcf
duplication
mutations
updated 3.2 years ago by
Pierre Lindenbaum
166k • written 3.2 years ago by
langzvi
• 0
1
vote
1
reply
670
views
Finding common pattern among heterogenous group of cancer
rnaseq
sequencing
updated 3.2 years ago by
Matthias Zepper
5.1k • written 3.2 years ago by
Hyper_Odin
▴ 320
0
votes
2
replies
1.6k
views
Clustered, annotated dotplot to scRNA-Seq data
scRNA-Seq
dotplot
visualization
updated 3.2 years ago by
Friederike
9.0k • written 3.2 years ago by
tomer9w
• 0
0
votes
3
replies
1.7k
views
Snakemake cluster execution error
snakemake
cluster
conda
updated 3.2 years ago by
Ram
45k • written 3.2 years ago by
blackadder
▴ 30
0
votes
1
reply
781
views
doubts about SNAP, bioinformatic tools for gene prediction
gene
prediction
updated 3.2 years ago by
lieven.sterck
15k • written 3.2 years ago by
JUAN LUIS
• 0
0
votes
1
reply
770
views
Computationally generated transcriptional regulation network
GRN
updated 3.2 years ago by
Matthias Zepper
5.1k • written 3.2 years ago by
nyanovsky
• 0
2
votes
6
replies
2.2k
views
Forum:
Getting the best of RNA-Seq
RNA-Seq
isoform
gene
expression
3.2 years ago by
Antonio R. Franco
★ 5.2k
0
votes
0
replies
639
views
News:
online training - Data Visualization with Python
Python
Data-Visualization
updated 3.2 years ago by
Ram
45k • written 3.2 years ago by
Physalia-courses
★ 2.6k
0
votes
1
reply
1.6k
views
How to count the number of multimapped reads from a bam file?
rnaseq
mapping
bowtie2
featurecounts
updated 3.2 years ago by
Shred
★ 1.6k • written 3.2 years ago by
O.rka
▴ 750
0
votes
2
replies
2.7k
views
How to find average read length and number of reads in a bam file using samtools in linux?
samtools
bam
updated 2.2 years ago by
Ram
45k • written 3.2 years ago by
MobiusT
▴ 20
1
vote
2
replies
803
views
Tool similar to CollectGcBiasMetrics
picard
updated 2.8 years ago by
Ram
45k • written 3.2 years ago by
tea.vuki
▴ 20
1
vote
5
replies
2.0k
views
Align short sequence against ONT reads
long-reads
ONT
alignment
genome
updated 17 months ago by
Ram
45k • written 3.2 years ago by
kirillkirilenko
▴ 40
1
vote
0
replies
805
views
Gene ontology enrichment vs. REACTOME pathway analysis
GO
REACTOME
3.2 years ago by
Gene_MMP8
▴ 240
0
votes
0
replies
838
views
News:
Cellosaurus release 42 is available
line
cell
biocuration
knowledgebase
database
3.2 years ago by
Amos Bairoch
▴ 140
0
votes
0
replies
521
views
extract rRNA/tRNA and other ncRNA ratio in a table from small RNA-seq
non-coding
small
RNA-seq
miRNA
analysis
RNA
clustering
3.2 years ago by
Rey
• 0
0
votes
0
replies
473
views
TCGA CIMP status
COAD
TCGA
updated 2.7 years ago by
Ram
45k • written 3.2 years ago by
ilomilo
▴ 10
121,844 results • Page
407 of 2437
Recent Votes
Comment: RNAseq requirements: Biological and Technical replicates
Comment: Feedback needed on new user-friendly BED file tool
Answer: CBioPortal: What does Mutation type: Targeted_Region means?
Comment: Tools for raw reads that estimate the percentage of reads that hit marker genes
BedToIntervalList (Picard) and IntervalListTools (Picard)
Answer: HIV virus - GTF annonation
Answer: Parabricks : Number of GPUs requested (2) is more than number of GPUs (0) in the
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★ 2.4k
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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…
Comment: RNAseq requirements: Biological and Technical replicates
by
ATpoint
89k
What is a technical replicate to you? A repeated library prep on the same pool of RNA? If so then no, I don't see the point as downstream a…
Comment: Feedback needed on new user-friendly BED file tool
by
ATpoint
89k
What I said already: Don't reimplement, wrap existing tools. I just tried some corrupted files (malformatted), and it threw no errors. It s…
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