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1 vote
1 answer
126 views

How to subset a large BAM file using BED file?

I have few NIST BAM files which require to be filtered for reads that are overlapping regions with the BED file. I have tried the following command using samtools: ...
Thanujay Suthahar's user avatar
4 votes
0 answers
43 views

Understanding NCBI eutils API results

I have made a Python function that can turn an NCBI GEO identifier (GSExxxxxx) into an ENA bioproject accession using the NCBI API. I need this to get sample tables which I then feed into Snakemake. ...
Freek's user avatar
  • 767
1 vote
0 answers
36 views

CRISPR Screen Alignments Mystery

I am analyzing a CRISPR screen. Illumina MiSeq, 5 million 75PE reads, and a PhiX spike in of 10%. The experiment is a depletion CRISPR library over time of a cell line. It is a subset of 700 guide ...
Question_question1137186218's user avatar
1 vote
0 answers
45 views

Add statistical test to this ggplot boxplot in R

Good morning, I was wondering if anyone could assist me with the following: I am struggling to add a statistical test to this boxplot like a bar (preferably with Wilcox test). I tried with adding ...
Nona's user avatar
  • 65
1 vote
2 answers
18 views

Will Cytoscape allow me to draw a network piece by piece and test claimed interactions?

As a scientific editor, I sometimes need to envisage proposed gene–enzyme–metabolite networks while editing papers. Being a visual thinker, I have to plot the claimed interactions and effects (as ...
BGHF's user avatar
  • 11
0 votes
0 answers
28 views

Choosing between Intel and AMD for bioinformatics and molecular dynamics workflows on Linux

I’m in the process of building a workstation for scientific computing, primarily focused on bioinformatics and molecular dynamics simulations. My daily tasks include: • Genome assembly and ...
Gilmar Lopez Armenta's user avatar
3 votes
1 answer
31 views

Construction of 1000 genome phase 3 reference panel

Currently I'm learning to merge reference panel with WGS data to attain a more population-specific panel for imputation of SNP array data. But I face 1 issue, it is not clear how to construct ...
Easper One's user avatar
2 votes
1 answer
19 views

What tool to use for visualizing combined TF binding sites and H3K27me3 enrichment across multiple cell lines using deepTools?

I'm analyzing ChIP-seq data for the transcription factor of interest (TF) and the H3K27me3 histone modification across three different cell lines: H9, HSMM, and iPSC. For each cell line, I have: TF ...
Dmitrii Trubetskoy's user avatar
1 vote
0 answers
32 views

STACKS process_radtags for demultiplexing RAD-seq data returning 57.5% "barcode not found" drops, retaining only 41.2% of reads

I'm having a very specific issue with demultiplexing my single-digest RAD-seq data using STACKS process_radtags. I have 389 individuals across 5 different libraries,...
rockygator's user avatar
-1 votes
0 answers
19 views

How to respond the comment on the sample size in qPCR

In my bioinformatics article, I discuss the identification of MEG3 and MAPK3 as potential therapeutic targets for osteoarthritis prognosis. In the experimental stage, Tissue samples from three case ...
wallace's user avatar
0 votes
0 answers
20 views

Cytoscape stringapp takes too much time getting protein queries and cloudflare's servers time out

I'm trying to load a list of 19153 genes in Cytoscape with the stringapp protein query, but since the list is gigantic, it takes a lot of time to gather all the protein names and cloudflare's server ...
Bobby's user avatar
  • 1
0 votes
0 answers
20 views

Warning in bcftools when subsetting a VCF by variant ID

I have successfully subset a VCF by variant ID after phasing and imputing using Beagle 5.5, however, I am getting the warning "[W::vcf_parse_info] INFO 'END' is not defined in the header, ...
Mubita 's user avatar
3 votes
1 answer
15 views

Getting organism information from the ENA API

I have been generating Snakemake sample tables from a GEO identifier (GSExxxxxx) directly by making requests to the NCBI and ENA APIs. It works, but with some caveats (explained in this open question: ...
Freek's user avatar
  • 767
0 votes
1 answer
19 views

Combining SCTransform, FindIntegrationAnchors, and Harmony

I'm trying to integrate 9 scRNA datasets from different publications. When using SCTranform combined with IntegrateData using anchors, the resulting UMAP is fairly noisy with some clear batch effect. ...
CellMacabre's user avatar
1 vote
0 answers
14 views

Unable to install cytoscape on the new version of sequoia (15.4.1)

I get this error message when trying to open the installer: You can’t open the application “Cytoscape Installer” because this application is not supported on this Mac. I am pretty sure this is ...
Joe's user avatar
  • 11

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