Extract multiple protein sequences from a Protein Data Bank along with Secondary Structure
Detect large deletions from CIGAR string
Re-use rules and avoid CyclicGraphException with snakemake
Fastest way to add Ns to variable length sequences such that they all equal 150bp
Mapping microarray probes
Trying to predict binding to lipopolysaccharide (LPS)
Error in breseq during running bowtie2
Converting .fasta files to .gff3 files
Find TopHat accepted_hits.bam mapped to transcriptome and genome separetly
How to process mach formatted, imputed genotyes (ENIGMA) with plink
Mauve on Ubuntu 16
Is it possible to pass a string variable to a BLAST search instead of a file?
Calculate (mean) sequence divergence for many sequences
Representing negative data on a log scle in Flow Cytometry
How to order multiple Fasta alignment files
Bam file error : No mithochondrial chromosome detected from the header
From the concatenated fasta file, how to find individual range of locations in each protein sequence
Bioinformatics: How do a contrast Limma with 3 groups (case/control, age and gender)
Unrecognized option: I picard.jar
How to use SAMtool htslib library to read optional info fields
How to use htslib/samtools to transform SAM/BAM reads?
Counting DNA Nucleotides using perl 6
ChemSpider refuses to accept the .MOL file I present it
How to count sequences in a fasta file using Bioperl
How to get taxonomic specific ids for kingdom, phylum, class, order, family, genus and species from taxid?
Biopython upgma tree construction is not giving ultrametric tree
Nucleotides separator in the pairwise sequence alignment bio python
how comparing PQG with PEG and PQA in Blast Algorithm?
How to get sequence description from gi number through biopython?
How to translate multiple fasta sequences?
Building Bowtie index failure (tophat2, bowtie2)
Looking at the results of clustering algorithms on Protein Interaction Networks
If operator inside for loop
Different results with MACS2 when Peakcalling with .bed or .bam
Is it possible to have an additional column of % similarity in the BLAST 2.2.26 output file?
Changing the record id in a FASTA file using BioPython
sort fastq file and keep sequences 15-17 bp in length
Computing pair wise distances for metabolic models
In bioinformatics, what is a singleton?
Beginner GWAS topic: virtual box command line can't find .ped file?
How to fix both the branch length and topology in MrBayes
how to convert a clusterw .dnd file to image (png) file?
How does Biopython determine the root of a phylogenetic tree?
How do I run MetaVelvet? The 'Getting Started' instructions don't work as expected
chip-seq alignment with multimach reads
Multiple sequence alignment. Convert multi-line format to single-line format?
Galaxy localhost reference data uploading
BLAST: blastpgp not producing an output file, unsure if using database flag correctly
How to run Mugsy multiple alignment software on Linux Ubuntu 11.04?
BioPython: Residues size differ from position
Clusters of Orthologous Groups [Software]
Send a Flat file attachment in the workflow in Informatica Developer
How to find ALL optimal local alignments using Smith-Waterman?
Is there a way to retrieve a list of annotations from Apache UIMA rather than using the CAS GUI?
How to convert fasta files (.fa) to gtf files for transcriptome assembly [closed]
Retrieving DNA sequences from a database of protein sequences?
In biopython, how can i get the 100% identity aligment?
Building .sif file from microarray ,tab file with expression valuses and gene id only
segmentation fault with SIFT
Flux simulator genome data processing
Reconstruction hierarchical model of miRNA transcription factor from miRNA microarray expression data?
How to change long gene names to abbreviated in some automatic way (microarray data processing)?
Conversion of Bowtie and Sam format alignment files
Get fasta source file from blast database name
Algorithm or requirement behind Bowtie?
ORF and amino identification using BioPython's translate() method— incorrect translations?
compute the distance between coordinates
How to fetch all records using NCBI Batch Entrez
How solve Fortran runtime error using Amber12
ChIP-seq data processing and the output of the program SPP
How to create 3D DNA Origami struture using cadnano
Why does Pubmed entrez tool for pmid 2 pmcid give weird results
Where can I find instructions on basic RNAseq data analysis? [closed]
Gene Ontology term Level vs. Gene Ontology term Type
Finding RNAs and information in a region
SNP ID conversion