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311 results • Page
1 of 7
Sort: Views
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Views
Votes
Replies
0
votes
1
reply
2.8k
views
RNA-seq compare FPKM's or fold change of different organisms
gene-expression
FPKM
RNA-seq
fold-change
updated 14 days ago by
Ram
40k • written 6.2 years ago by
jehu
▴ 30
2
votes
10
replies
2.8k
views
6 follow
Split plink files by a number of SNPs
GWAS
SNP
plink
updated 1 day ago by
Raygozak
★ 1.4k • written 5.2 years ago by
kakukeshi
▴ 80
0
votes
7
replies
2.7k
views
qPCR: Huge variation in fold change of genes between biological replicates
qpcr
fold-change
updated 14 days ago by
Ram
40k • written 5.3 years ago by
AP
▴ 80
3
votes
3
replies
2.2k
views
WGCNA Labeled Heatmap
heatmap
wgcna
updated 3 days ago by
Ram
40k • written 2.0 years ago by
Anand
▴ 40
0
votes
3
replies
2.0k
views
extraction of original gene iDs from reference annotation file
rna-seq
updated 10 days ago by
aishwarya
• 0 • written 5.3 years ago by
blooming.daisy333
▴ 110
0
votes
2
replies
2.0k
views
CWL :File created on fly by one step of a workflow as input to another step
Common-Workflow-Language
CWL
updated 18 days ago by
Ram
40k • written 6.5 years ago by
akashmdr90
• 0
0
votes
1
reply
1.7k
views
error when running local chlorop1.1
chlorop
updated 5 days ago by
Ram
40k • written 7.3 years ago by
gerrychang1985
▴ 40
8
votes
5
replies
1.6k
views
BLASTp command line : filtering results by a minimum % of identity and % coverage
BLASTp
updated 8 days ago by
Ram
40k • written 24 months ago by
A_heath
▴ 140
2
votes
20
replies
1.6k
views
The number of SVs called by `vg call` is much smaller than the number of SVs in the VCF used to construct the graph
vg
23 days ago by
Maxine
▴ 30
0
votes
2
replies
1.6k
views
Question about REDItools
REDItools
updated 14 days ago by
Ethan Lee
• 0 • written 4.1 years ago by
tujuchuanli
▴ 100
2
votes
13
replies
1.5k
views
RepeatMasker error when trying to generate repeat sequence distribution pie chart (all code and errors provided)
repeatmasker
updated 3 days ago by
Ram
40k • written 6 weeks ago by
epianalysis
• 0
2
votes
3
replies
1.5k
views
Racon command line with paired-ends Illumina reads
Illumina
Racon
updated 8 days ago by
Ram
40k • written 2.1 years ago by
A_heath
▴ 140
0
votes
1
reply
1.4k
views
NS, AC, AN and AF in VCF file
VCF
updated 25 days ago by
Mwangana
• 0 • written 14 months ago by
wangdp123
▴ 310
0
votes
1
reply
1.0k
views
Downstream analysis on multi-sample or single-sample VCF files?
next-gen
VCF
updated 14 days ago by
Ram
40k • written 2.8 years ago by
NGSCanBioinf
▴ 10
0
votes
9
replies
1.0k
views
Chipseq analysis on repeat genes
galaxy
repeatmasker
ChIP-seq
repeat-elements
ATAC-seq
updated 3 days ago by
rfran010
▴ 830 • written 15 days ago by
pb11
▴ 10
3
votes
5
replies
1.0k
views
Running purge_dups on a hybrid assembly (optical mapping + reads)
pacbio
purge_dups
Assembly
bionano
updated 16 days ago by
colindaven
5.5k • written 2.7 years ago by
pablo
▴ 280
1
vote
1
reply
995
views
SCENIC-openloom not working
sc-rna
SCENIC
sequencing
updated 5 days ago by
kyriakds
• 0 • written 2.1 years ago by
Lekshmy
▴ 10
1
vote
5
replies
961
views
What statistical test to apply for DE after CibersortX deconvolution
cibersortx
differential-expression
t-test
deconvolution
18 days ago by
Sam
▴ 290
0
votes
7
replies
940
views
FACS (Fluorescence-activated cell sorting NOT cyTOF),Automating the removal of dead and duplicated cells
FACS
updated 3 days ago by
rfran010
▴ 830 • written 17 days ago by
ccbb7aab4
▴ 20
1
vote
10
replies
915
views
Deepvariant variant calling by singularity
deepvariant
singularity
conda
docker
updated 7 days ago by
jeffhsu3
• 0 • written 12 weeks ago by
fra.silvestro99
▴ 10
0
votes
1
reply
910
views
Issue interpreting plasmidSPAdes output
plasmidSPAdes
updated 8 days ago by
Ram
40k • written 2.9 years ago by
A_heath
▴ 140
0
votes
7
replies
791
views
Mugsy error -directory must be a directory
Mugsy
updated 8 days ago by
Ram
40k • written 2.8 years ago by
A_heath
▴ 140
1
vote
11
replies
789
views
Quantification after transcriptome assembly with Trinity
De-novo-transcriptome-assembly
Trinity
RNA-seq-analysis
updated 5 days ago by
GenoMax
134k • written 4 weeks ago by
langziv
▴ 50
0
votes
1
reply
762
views
How to identify specific region using Mauve?
Mauve
primers
updated 8 days ago by
Ram
40k • written 2.8 years ago by
A_heath
▴ 140
0
votes
11
replies
750
views
Normalization for microarrays >1000+ samples?
microarray
normalization
oligo
9 days ago by
evmae
• 0
0
votes
3
replies
735
views
How to add translation of CDS in Artemis?
translation
Artemis
updated 8 days ago by
Ram
40k • written 2.7 years ago by
A_heath
▴ 140
15
votes
16
replies
722
views
ncbi error report log for validate fastq issue
sra-tools
updated 2 days ago by
GenoMax
134k • written 3 days ago by
1769mkc
★ 1.1k
0
votes
3
replies
720
views
to annotate BEDPE files
bedtools
annotate
updated 3 days ago by
Lhl
▴ 760 • written 2.6 years ago by
Bogdan
★ 1.4k
0
votes
2
replies
698
views
pal2nal -nogap -nomismatch options not working
pal2nal
updated 14 days ago by
wangjb702
• 0 • written 10 months ago by
pkfsantos
• 0
0
votes
2
replies
696
views
RSEM not giving .genes.results and isoforms.results ; Plase check if you provide correct parameters/options for the pipeline!
genomics
transcriptome
rsem
ngs
2 days ago by
kat.bi
• 0
0
votes
0
replies
693
views
Is it possible to combine count gene expression data coming from one sequencing technology (RNA seq) with intensity gene expression data coming from …
Differential-expression
Normalization
updated 29 days ago by
Ram
40k • written 4 weeks ago by
Sep
• 0
2
votes
7
replies
690
views
VG mapping paired-end reads: error [xg]: multiple hits for XXX
variation-graph
reads
pangenome
vg
paired-end
26 days ago by
nkls063408
• 0
1
vote
3
replies
673
views
How to determine plasmid or chromosomal origin?
plasmid
chromosomal-origin
updated 8 days ago by
Ram
40k • written 3.0 years ago by
A_heath
▴ 140
1
vote
5
replies
672
views
Mugsy percentage of identity
Mugsy
Genome-alignment
updated 8 days ago by
Ram
40k • written 2.6 years ago by
A_heath
▴ 140
0
votes
1
reply
659
views
How to get enrichment of ERVs in differentially expressed peaks from ATAC-seq data?
ChIP-Seq
ERVs
ATAC-seq
updated 14 days ago by
pb11
▴ 10 • written 2.8 years ago by
fdemiguelsdp
• 0
0
votes
4
replies
634
views
CAZy database has multiple family sequence...
metagenomics
cazy
annotation
updated 23 days ago by
JyiYeung
• 0 • written 9 months ago by
GYUDAE
• 0
0
votes
0
replies
626
views
How can I summarize Log2 Fold Change values for many genes within a treatment group?
fold-change
updated 14 days ago by
Ram
40k • written 2.4 years ago by
sagrant
▴ 10
2
votes
7
replies
602
views
Weirdness in annotation (missing allele frequencies)
allele-frequency
gnomad
annovar
updated 46 minutes ago by
Jeremy Leipzig
21k • written 8 days ago by
Can Abdullah
• 0
0
votes
0
replies
596
views
Contig extension using PRICE
price
updated 8 days ago by
Ram
40k • written 3.0 years ago by
A_heath
▴ 140
0
votes
5
replies
591
views
Bowtie2 with secondary alignment option produces multiple mapping with offset and varying alignment scores
bowtie2
score
alignment
multiple-alignment
26 days ago by
polag01
▴ 10
0
votes
13
replies
588
views
STAR Intron Motif Script Gives Segmentation fault Error
STAR
Linux
6 days ago by
Y
• 0
0
votes
0
replies
558
views
after gatk VariantAnnotator -V *_com_norm.vcf -A AlleleFraction -O *_norm_AB.vcf There "nan,nan" or "nan" in my vcf file
gatk
AlleleFraction
VariantAnnotator
updated 11 days ago by
Ram
40k • written 11 days ago by
zhuo
• 0
0
votes
2
replies
556
views
Network analysis for two Factors
chip-seq
network-analysis
updated 28 days ago by
Ram
40k • written 7 months ago by
Ankit
▴ 390
3
votes
5
replies
542
views
Neither pysam nor samtools reading HTTPS-sourced BAM file correctly
bam
pysam
samtools
updated 26 days ago by
Istvan Albert
98k • written 28 days ago by
Alex Reynolds
35k
3
votes
10
replies
526
views
STAR index not working
STAR
RNA-Seq
8 days ago by
camillab.
▴ 140
1
vote
5
replies
519
views
Idat raw data conversion
idat
updated 12 days ago by
Giulio Genovese
▴ 330 • written 14 days ago by
Zi
• 0
4
votes
5
replies
507
views
Pre-processing for single cell RNAseq: Hard thresholds, data (cluster)-driven or both?
scRNA-seq
12 days ago by
psm
▴ 100
1
vote
1
reply
489
views
Haplogrep classify error
haplogroup
mitochondria
haplogrep
updated 19 days ago by
angelika_95
• 0 • written 2.0 years ago by
jdru
▴ 10
0
votes
5
replies
477
views
Convert gene id's to gene symbol preserving gene id's in deseq2
ensembl
r
DE
deseq2
updated 13 days ago by
Ram
40k • written 15 days ago by
dylannicoembros
• 0
2
votes
9
replies
474
views
Calculation of TMB on gene level
genomics
updated 4 days ago by
svp
▴ 590 • written 5 days ago by
smrutimayipanda
▴ 20
311 results • Page
1 of 7
Recent Votes
A: running RAxML and MrBayes over concatinated multiple sequence alignments
Comment: Weirdness in annotation (missing allele frequencies)
Comment: Weirdness in annotation (missing allele frequencies)
Comment: ncbi error report log for validate fastq issue
Comment: ncbi error report log for validate fastq issue
A: Bowtie2 MAPQ difference using local vs end-to-end alignment
C: Bowtie2 MAPQ difference using local vs end-to-end alignment
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Recent Replies
Comment: Weirdness in annotation (missing allele frequencies)
by
Jeremy Leipzig
21k
0.60625 is 97/160 so if you have 80 individuals in your VCF that's an internal allele frequency, not gnomAD
Comment: Weirdness in annotation (missing allele frequencies)
by
Can Abdullah
• 0
Yes, I was confused as well. I think the same. Maybe Annovar uses some other resources besides gnomad, but it does not make sense. Also, I …
Comment: Weirdness in annotation (missing allele frequencies)
by
Can Abdullah
• 0
Thank you so much, I decided to move forward as you suggested. Initially, I thought using the most up-to-date databases and positions would…
Comment: Getting the overlap between two GTF files
by
GenoMax
134k
Something in `AGAT` should work: https://agat.readthedocs.io/en/latest/?badge=latest
Answer: Automate the Splitting of a VCF File by Sample (bcftools)
by
Pierre Lindenbaum
157k
> My problem has been with trying to loop the process. ok here is a **nextflow** based solution,(NOT tested) workflow { …
Comment: Assessing Rockhopper's output
by
langziv
▴ 50
I see. I tried using the GUI Rockhopper for RNA-seq analysis of a K. pneumoniae strain, but the program didn't find the strain's assembly…
Answer: Getting the overlap between two GTF files
by
Pierre Lindenbaum
157k
bedtools intersect \ -a <(awk '/^[^#]/ {printf("%s\t%d\t%s\t%s\n",$1,int($4)-1,$5,$0);}' file1.gtf | sort -t $'\t' -k1,1 -k2…
Comment: Assessing Rockhopper's output
by
shelkmike
▴ 980
I used Rockhopper only for bacterial genomes assembled into circular contigs or circular scaffolds.
Comment: Unable to install HorvathMammalMethylChip40manifest packages
by
ATpoint
77k
There is no package of that name in CRAN or Bioconductor. Where do you have it from, so which tutorial you follow?
Comment: Subclustering of intergated cells from scRNA-seq data
by
fifty_fifty
▴ 60
thank you. This is exactly what I was looking for
Answer: Search RCSB with a list of protein names?
by
Mensur Dlakic
★ 25k
This is not the most elegant solution, but it should work with previous suggestions. In this remote directory: http://ftp.wwpdb.org/p…
Answer: Automate the Splitting of a VCF File by Sample (bcftools)
by
Ram
40k
The manual says you can split samples out at once using the `+split` plugin. So, `bcftools +split -Oz -o <PATH> file.vcf.gz` should do the …
Comment: differences between trajectories in conditions with Monocle3 or other tools
by
Amitm
★ 2.2k
Phate (or Monocle) doesn't do UMAP. If you have done UMAP already (using seurat) then you could use the cell barcode to UMAP cluster label …
Comment: Error: cannot open file 2 for reading From Cufflinks Version 2.2.1 When Attempti
by
Y
• 0
I figured out how to make it work. The bams have to be comma separated not just by space: cd "${input_directory_with_associated_bam_fi…
Comment: Search RCSB with a list of protein names?
by
Joseph
• 0
Hey, this is so close to what I'm looking for - I clarified in my edit. This is a great way to batch download lots of PDBs in RCSB by their…
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