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First question with score of 1 or more.
Awarded 884 times.
Why does samtools mpileup sometimes include ref bases (other than ',' or '.')?
Awarded 17 hours ago
How to deal with zeros in the denominator when calculating percent enrichment?
Awarded yesterday
Do additional peaks in percent GC of PacBio gDNA reads indicate contamination?
Awarded yesterday
Trying to divide number in fourth TSV column by a certain number according to its corresponding identifier in the first column
Awarded yesterday
Can someone recommend software for reference-based genotype-estimation?
Awarded Feb 24 at 20:30
Database with antigens and current vaccines
Awarded Feb 24 at 16:45
What are the different kinds of bioluminescent genes?
Awarded Feb 23 at 10:05
Distinguishing Splicings that Produce Functional Transcripts Amongst Alternates Shown
Awarded Feb 22 at 19:30
Identifying mutually **exclusive** gene sets
Awarded Feb 21 at 17:35
How to filter a SAM file by a bed file?
Awarded Feb 21 at 10:05
Protein ligand docking: how to convert <protein>.pdb to <protein>.maps.fld?
Awarded Feb 21 at 7:55
What's the difference between Procheck and Whatcheck?
Awarded Feb 20 at 23:45
How to initiate RNA-Seq analysis of TCGA files?
Awarded Feb 20 at 5:55
How can I find genes of fundamental metabolic processes for an organism?
Awarded Feb 20 at 5:10
Scientific names of taxids with kraken 2.0.8 beta, command kraken2 --use-names error
Awarded Feb 20 at 5:10
How can i get data set of illness and not illness people?
Awarded Feb 20 at 4:50
bwt suffix array construction
Awarded Feb 20 at 4:50
How to create a .phy file for constructing a phylogenetic tree?
Awarded Feb 18 at 23:00
select unique names while removing the duplicates from a column
Awarded Feb 18 at 10:05
Using cellranger for non-10x data
Awarded Feb 17 at 12:10
How to calculate Centimorgan lengths from run lengths in one-to-one dna profile comparison
Awarded Feb 17 at 10:00
Why do these NCBI representative genomes for ape species have no Y chromosome?
Awarded Feb 13 at 22:55
Running tophat dockerfile in background
Awarded Feb 13 at 0:45
Calculating the mortality rate of a pandemic, e.g. coronavirus 2019-nCov?
Awarded Feb 12 at 18:10
Algorithmic Information Measurement of Human Genome Databases?
Awarded Feb 12 at 10:00
How to find a homolog that has a PDB structure available
Awarded Feb 11 at 22:45
No output when trying to obtain protein sequence from PDB file
Awarded Feb 11 at 11:20
Can I submit a R package to Bioconductor or CRAN if I have already published it a journal?
Awarded Feb 10 at 15:30
Writing a python module to run Infernal on a list of fasta files
Awarded Feb 10 at 13:15
Why does the FASTA sequence for coronavirus look like DNA, not RNA?
Awarded Feb 9 at 21:40
How to translate amino acid sequences to Nucleotide sequences
Awarded Feb 9 at 10:35
Differential gene expression bias due to effect of an individual sample
Awarded Feb 6 at 16:00
Is it possible for coronavirus or SARS to be synthetic?
Awarded Feb 4 at 22:00
Looking for a way to download all pdb files that detail a protein-drug complex
Awarded Feb 3 at 15:25
Bedtools wrongly indicates zero coverage
Awarded Feb 1 at 15:40
A new paper suggests the Corona Virus has “Uncanny similarity of unique inserts in the 2019-nCoV spike protein to HIV-1” - What does this mean?
Awarded Jan 31 at 21:00
Interpretion of my coronavirus 2019-nCov, Wuhan, China BLAST tree?
Awarded Jan 27 at 23:55
Ancestry of the coronavirus 2019-nCov, WuHan city, China
Awarded Jan 27 at 23:50
how to calculate coverage of each base of mapped reads?
Awarded Jan 27 at 17:40
Pulling out a certain gene in a volcano plot
Awarded Jan 25 at 20:50
Finding simple sequence from reads with significant overlap
Awarded Jan 17 at 4:50
Tool for calibrating base quality scores?
Awarded Jan 13 at 15:15
Existing tool for converting gff3 to genbank (gbk)
Awarded Jan 13 at 14:15
Genetic Genealogy related to SNP variants and INDEL variants
Awarded Jan 13 at 14:15
Any user friendly way to find rare mutations in whole genome raw?
Awarded Jan 13 at 14:10
NA12878 equivalent for somatic variant calling [duplicate]
Awarded Jan 9 at 20:55
Seurat FindMarkers() output, percentage
Awarded Jan 9 at 17:10
Why I am getting different gene lengths for the same genes in different samples with rsem-calculate-expression?
Awarded Jan 8 at 14:00
Infer the new (Ban et. al) ribosomal nomenlature (ex. uL53 ) from the ribosomal protein's sequence
Awarded Jan 5 at 16:50
Are there any “canonical” sources of C. Elegans connectome?
Awarded Jan 4 at 2:10
Median for clinical significance
Awarded Jan 1 at 1:55
What is a read count?
Awarded Dec 30 '19 at 21:10
How could I match atom orders between a .mol2 and a .pdb?
Awarded Dec 26 '19 at 13:20
Replicate papers (beginner) [closed]
Awarded Dec 25 '19 at 15:15
What is the significance of enrichment factor regarding machine learning methods?
Awarded Dec 24 '19 at 12:20
MiXCR: only create a single export file for all clonotypes
Awarded Dec 24 '19 at 5:35
How can I run a command for multiple files?
Awarded Dec 24 '19 at 5:05
How to do the reverse of bcf merge?
Awarded Dec 24 '19 at 5:00
pysam or piping samtools view to a python script
Awarded Dec 11 '19 at 22:50
Detect differentially expressing cells
Awarded Dec 9 '19 at 10:10
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