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329 results • Page
3 of 7
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Votes
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0
votes
0
replies
229
views
Can I visually see the file I read in .obj format in R?
3D
R
updated 4 days ago by
Ram
38k • written 8 months ago by
logbio
▴ 30
0
votes
1
reply
409
views
Bugs? on GSEA anaylsis
GSEA
updated 4 days ago by
Ram
38k • written 22 months ago by
jiasheng.zhong
• 0
0
votes
0
replies
192
views
How to find association between a gene-rsid and AD
association
Loci
LD
AD
5 days ago by
rheab1230
▴ 140
0
votes
2
replies
312
views
best practice to choose AF threshold based on population number
VCF
AF
allele-frequency
4 days ago by
prasundutta87
▴ 650
0
votes
0
replies
409
views
How can I make multiple taxID queries using qblast and store multiple blast handles using NCBIXML?
NCBIXML
qblast
python
biopython
updated 4 days ago by
Ram
38k • written 21 months ago by
oseias.rf.junior
• 0
0
votes
4
replies
603
views
Help needed
bioalcidae
updated 4 days ago by
Ram
38k • written 14 months ago by
Nai
▴ 50
0
votes
0
replies
138
views
Fine mapping with GWAS
PAINTOR
GWAS
FINE-MAP
POST-GWAS
updated 1 day ago by
Nicolas Rosewick
10k • written 1 day ago by
Swati
• 0
0
votes
0
replies
126
views
How would I assess evolutionary estimates between duplicated vs. non-duplicated genes in PAML?
PAML
2 days ago by
codoncity
• 0
0
votes
2
replies
374
views
Which database should I get variant data from WGS for Asian and AA populations
vcf
WGS
variant
database
updated 11 hours ago by
Ram
38k • written 8 months ago by
minghuiguo448
• 0
0
votes
0
replies
163
views
MEME motif discovery
fasta
updated 9 hours ago by
Ram
38k • written 10 months ago by
kaisakaiho73847
• 0
0
votes
0
replies
365
views
linkage disequilibrium and haplotype analysis of GWAS .
plink
plink1.9
GWAS
updated 4 days ago by
Ram
38k • written 19 months ago by
gdeep.14
• 0
0
votes
0
replies
171
views
How to export the result contents (analyzed part only) of clr function to the CSV file ? (The microbiota data) in R Aldex2 package
Aldex2
ASV
R
updated 4 days ago by
Ram
38k • written 5 days ago by
ohtang7
▴ 30
0
votes
2
replies
107
views
Creating loop for read groups using Picard
bash
picard
loop
updated 3 hours ago by
ntsopoul
▴ 20 • written 7 hours ago by
brandnewatthis
• 0
0
votes
0
replies
391
views
Universal Human Reference RNA Sample
RNA
updated 4 days ago by
Ram
38k • written 19 months ago by
kstangline
▴ 70
0
votes
1
reply
313
views
without using blast how we can What features distinguish the genomic DNA sequence
sequence
updated 4 days ago by
Ram
38k • written 8 months ago by
yasir
• 0
0
votes
2
replies
292
views
bed file question! [extract read numbers from bed file]
BED
updated 1 day ago by
Ram
38k • written 4 months ago by
Jjbox
▴ 40
0
votes
2
replies
370
views
Error message while running Stats.sh
Stats.sh
updated 4 days ago by
Ram
38k • written 7 months ago by
sabreenaalam12345
• 0
0
votes
0
replies
68
views
Homer annotatePeaks for enrichment analysis
annotatePeaks
homer
DMR
methylation
18 hours ago by
Joana
• 0
0
votes
2
replies
297
views
Trouble using Human_GeCKOv2_Library_combine.csv to run MAGeCK
nontarget-sgrna
MAGeCK
updated 1 day ago by
Ram
38k • written 8 months ago by
teresa
• 0
0
votes
0
replies
88
views
Add HI:i:<n> tag to a BAM file
SAM
hisat2
STAR
tag
BAM
19 hours ago by
predeus
★ 1.8k
0
votes
0
replies
118
views
Dnaplotter
Artemis
22 hours ago by
prs
• 0
0
votes
0
replies
1.7k
views
How to calculate LD in 2 direction?
SNP
updated 1 day ago by
Ram
38k • written 8.0 years ago by
mandecent.gupta
• 0
0
votes
4
replies
582
views
I want to merge gene sequences in fasta to create one genome from all cds region.
fasta
linux
genome
updated 1 day ago by
Ram
38k • written 10 weeks ago by
iankeetkumar
• 0
0
votes
2
replies
308
views
When do the PCR Bottlenecking Coefficient
PCR
bam
chip-seq
updated 1 day ago by
Ram
38k • written 10 weeks ago by
michelafrancesconi9
• 0
0
votes
0
replies
627
views
qBLAST run and Multiple sequence alignment
XML
alignment
qblast
sequence
updated 4 days ago by
Ram
38k • written 2.3 years ago by
gurilion007
• 0
0
votes
0
replies
101
views
Seeking explanation of the difference between GO term normal vs non-redundant!
GO
RNA-seq
term
analysis
webgestalt
6 days ago by
Soumajit
▴ 30
0
votes
0
replies
3.5k
views
Which keytype from org.Mm.eg.db match the annotations in the ensembl gtf file?
RNA-Seq
DESeq2
updated 4 days ago by
Ram
38k • written 5.1 years ago by
alejandro.colaneri
▴ 10
0
votes
0
replies
70
views
PGx question regarding RSIDs with more than one variant associated with it
pharmacogenomics
rsid
pgx
1 day ago by
Roy
▴ 10
0
votes
0
replies
188
views
PSL file confusion on negative strand
BLAT
PSL
updated 11 hours ago by
Ram
38k • written 8 months ago by
spark
• 0
0
votes
1
reply
384
views
Open source projects
programming
updated 4 days ago by
Ram
38k • written 13 months ago by
Sam
• 0
0
votes
1
reply
235
views
Conformational antigens
Immunoinformatics
updated 4 days ago by
Ram
38k • written 4 days ago by
Mohamed
• 0
0
votes
1
reply
229
views
RNA-seq using rasflow - issues with annotation file
gtf
rasflow
gff
RNA-seq
updated 4 days ago by
Ram
38k • written 5 months ago by
cdeantoneo31
▴ 10
0
votes
2
replies
185
views
Processing fastqs generated by inDrop protocol
single-cell
rna-seq
indrop
updated 1 day ago by
Ram
38k • written 1 day ago by
bobbybobbobbo
• 0
0
votes
1
reply
242
views
comparison between STARsolo and cellranger
STARsolo
cellranger
updated 4 days ago by
GenoMax
127k • written 4 days ago by
dalibenam64
• 0
0
votes
2
replies
744
views
minor allele frequency graph
maf
SNP
updated 14 hours ago by
Ram
38k • written 2.3 years ago by
bioinfonewbie
• 0
0
votes
1
reply
190
views
How to obtain unmapped reads from the paired end samples using hisat2
fastq
hisat2
updated 1 day ago by
Ram
38k • written 8 weeks ago by
otieno43
• 0
0
votes
0
replies
203
views
conversion between branch length to SNP numbers
SNPs
Phylogeny
updated 4 days ago by
Ram
38k • written 10 months ago by
beckyrjb6
▴ 20
0
votes
0
replies
151
views
pyscenic
pyscenic
scenic
2 days ago by
Andy
▴ 30
0
votes
4
replies
324
views
WGCNA number of modules issue
networks
gene
WGCNA
correlation
5 days ago by
1215045934
▴ 80
0
votes
0
replies
140
views
How to detect tumor-specific splicing aberrations
splicing
6 days ago by
iraun
5.8k
0
votes
1
reply
2.1k
views
How would sequence overrepresentation and duplication level affect the quality of a De Novo transcriptome assembly?
next-gen
Assembly
Trinity
RNA-Seq
updated 1 day ago by
Ram
38k • written 7.9 years ago by
guillermo.ponz.segrelles
▴ 20
0
votes
0
replies
388
views
Need help interpreting CoGe SynMap result
genome
genomics
updated 5 days ago by
Ram
38k • written 20 months ago by
Lucas Peres
▴ 80
0
votes
2
replies
639
views
Samtools view error: header include @SQ line missing LN tag.
minimap2
updated 4 days ago by
Ram
38k • written 23 months ago by
Digimon
• 0
0
votes
7
replies
1.1k
views
Unable to convert from sam to bam file.
bam
sam
samtools
updated 8 hours ago by
Ram
38k • written 14 months ago by
usef
• 0
0
votes
0
replies
455
views
How to plot heatmap for the matrix for the pairwise comparison of sequence similarity in python?
heatmap
python
distance-matrix
updated 8 hours ago by
Ram
38k • written 15 months ago by
ramsha
• 0
0
votes
0
replies
137
views
Differential (pathways) expression testing using linear model packages in R (Limma & GSVA)
GSVA
limma
R
1 day ago by
Tadeoye
▴ 30
0
votes
1
reply
152
views
mrbayes segmentation fault
mrbayes
segmentation
fault
updated 23 hours ago by
Mensur Dlakic
★ 23k • written 1 day ago by
dgrace999
• 0
0
votes
4
replies
689
views
How to download the final reads of SRA data from NCBI using fastq-dumb
fastq
fasta
SRA
updated 4 days ago by
Ram
38k • written 21 months ago by
FadyNabil
▴ 10
0
votes
1
reply
1.8k
views
bwa XA field: What is the procedure for the binning of all but one alternative alignments into XA?
sam
bwa
updated 4 days ago by
Ram
38k • written 6.3 years ago by
izaak.coleman1
▴ 30
0
votes
0
replies
127
views
check if a protein abundance is expected to be low
mass-spectrometry
5 days ago by
Abhishek
• 0
329 results • Page
3 of 7
Recent Votes
Answer: RNA-SEQ
Comment: RNA-SEQ
Comment: RNA-SEQ
Answer: RNA-SEQ
Gene Set Enrichment Analysis
Can I sort my bam files with Picard MergeSamFiles?
Answer: Problem generating a .vcf after upgrade of samtools and bcftools
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Answer: How to implement this two-stage one-to-many workflow using WDL?
by
Ruben
• 0
> Unfortunately, as far as I can tell, WDL provides no support for iterating over the contents of a directory. (I find this shocking. I con…
Answer: activity of unloaded/unassembled Tn5
by
callumjcparr
• 0
So I hope someone is still interested in this. We have taken to preparing recombinant Tn5 now as it's much cheaper than commercial suppli…
Comment: RNA-SEQ
by
ali
• 0
thanks for your helping
Comment: TSS of protein coding genes
by
ConvolutedGenome
▴ 10
I am quite confused with GENCODE GTF file, So, within the GENCODE GTF file, I noticed that each (protein-coding) gene has multiple "transc…
Comment: Recommendation for (Alternative) Splicing analysis packages for bulk RNA-seq da
by
iraun
5.8k
Hi! I personally use [SplAdder][1], in case you want to add it to your list :). [1]: https://github.com/ratschlab/spladder
Answer: Problem generating a .vcf after upgrade of samtools and bcftools
by
Andy
• 0
Really the only needed, that help worked, thank's
Comment: Active enhancers for mm39
by
seidel
11k
Just curious what you mean by "active" enhancers. Enhancers are active in a given context (e.g. cell type developmental state, etc.), and m…
Comment: Creating loop for read groups using Picard
by
ntsopoul
▴ 20
try absolute paths navigate to the directory with cd and use pwd to get the absolute directory.
Comment: how to create interacting Hi-C peaks
by
rheab1230
▴ 140
Thank you. I will use this package since I am more familiar with R
Comment: how to create interacting Hi-C peaks
by
rheab1230
▴ 140
thank you. i will go through it
Comment: Fastqc report analysis
by
npavliukovec
• 0
Yeah, after trimming and fastqc I will have to generate MultiQC plots and after do mapping with reference genome. As I know, for eukaryotes…
Comment: My fastq files(paired end) have different read number
by
kimgeng
• 0
Oh, I see, Thank you however, I want to make vcf files with gatk haplotypecaller and GenotypeGVCFs. But I got some problems I have about 2.…
Answer: My fastq files(paired end) have different read number
by
ntsopoul
▴ 20
Yes, this is normal because depending on how you generate the bam file, the non-aligning reads are saved in the .bam file along the properl…
Answer: Can I use abundance from Tximport to compare the expression level of transcript
by
ntsopoul
▴ 20
No, you should not do that since the count matrix is not normalized. Also, the statistics for getting a pValue requires consideration of al…
Comment: Easy way to split VCF file by chromosome
by
Joana
• 0
You need to run bcftools index on your vcf file before running the suggested command.
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