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<prev • 64,921 results • page 1 of 2165 • next >
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How to plot allele frequency
R snp written 20 minutes ago by mostafarafiepour • 50
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26
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How can i increase variants accuracy?
assembly alignment snp variants written 38 minutes ago by atiqueulalam • 0
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1
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421
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1
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High FPKM values for bacterial genes
rna-seq written 15 months ago by Cacau • 410 • updated 40 minutes ago by Biostar ♦♦ 20
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47
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Fasta file from a gff file
gene genome written 3 hours ago by ahmedferoz20 • 0
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5
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3.6k
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5
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Stuck creating reference genome with STAR
genome rna-seq written 2.8 years ago by nash.claire • 300 • updated 2 hours ago by valizad2 • 0
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STAR problem: EXITING because of INPUT ERROR: could not open genomeFastaFile:
alignment rna-seq written 2 hours ago by valizad2 • 0
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41
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training genemarkS to call proteins from virus genomes
annotation rna-seq genemark gene calling written 4 hours ago by Guillermo D. Huerta • 10
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66
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2
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Software for Unaligning Sequences
alignment written 7 hours ago by printingdots • 0 • updated 5 hours ago by Alex Reynolds ♦ 26k
376
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19
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29k
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173 follow
19
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News: The Biostar Handbook. A bioinformatics e-book for beginners.
tutorial news training handbook written 22 months ago by Istvan Albert ♦♦ 77k • updated 5 hours ago by RamRS ♦ 18k
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38
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Less number of motifs found in the real network when compared to the random network
network motif written 5 hours ago by The Last Word • 160
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R code for Differential Gene Expression
rna-seq written 11 hours ago by landrjos • 10 • updated 6 hours ago by Istvan Albert ♦♦ 77k
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58
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1
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Should I be worried about my data
sequence next-gen written 8 hours ago by will.wcb • 10 • updated 6 hours ago by Istvan Albert ♦♦ 77k
5
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1
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1.0k
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1
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Retrieving GO terms from ensembl bacteria
rest ensembl go terms gene ontology api written 21 months ago by Diego • 40 • updated 6 hours ago by Biostar ♦♦ 20
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55
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1
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How to use samtools tview goto with long reference sequence name
samtools goto reference tview written 7 hours ago by quokka • 0
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66
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Gene IDs turn into mutiple Ensembl IDs?
genome python ensembl written 8 hours ago by iannos • 0
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44
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Alt allele count from 1000 genome project
alt allele count 1000 genome written 7 hours ago by seta • 1.0k
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38
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(Closed) Difference between sensor cells and antigen presenting cells?
sensor cells apc dendritic cells written 9 hours ago by Superstar • 0
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52
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How to read an mpileup file from Samtools into Python
python next-gen samtools mpileup written 10 hours ago by M.O.L.S • 0
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775
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HHpred threading or homology ?
alignment sequence written 2.9 years ago by modmod • 0 • updated 12 hours ago by Biostar ♦♦ 20
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74
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1
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how to correct this Error while building index from .bam file?
.bam samtools index .bai mapping written 12 hours ago by jaqx008 • 40
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133
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1
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Connecting clusters of cells in 2 adjacent time points.
urd R adjacency matrix igrap seurat written 10 days ago by F • 3.1k
3
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1
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109
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1
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How to separate mixed orientation raw illumina sequence into forward and reverse fastqs?
sequence next-gen written 1 day ago by will.wcb • 10 • updated 14 hours ago by mike-zx • 100
3
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1
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83
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1
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Removing primers with degenerate codes
primers written 20 hours ago by life99945 • 0 • updated 15 hours ago by h.mon ♦ 20k
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82
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1
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size considerations CWL Toil workflow step inputs
toil cwl written 1 day ago by ionox0 • 200
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54
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Gene Paralogs from GeneCards or Genes Like Me
gene rna-seq written 17 hours ago by Chris_AI • 30
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262
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How to convert RNA-seq data to microarray data as if it was microarray data
microarray rna-seq written 7 weeks ago by shuyong • 0 • updated 18 hours ago by Biostar ♦♦ 20
9
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675
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7 follow
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News: Pan-Cancer Analysis of RNA Binding Proteins in ~7000 tumor samples
cancer driver rna-seq news tcga pan-cancer mutations written 9 months ago by lsp03yjh • 580
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93
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Draw gene-transcroption factor network starting from a list of gene
transcription factor written 1 day ago by english.server • 50
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1
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105
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1
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Convert colorspace fastq to basespace fastq
rna-seq written 1 day ago by aflrios • 0
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75
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Error for converting from gene symbol to Entrez IDs
"org.dr.eg.db" package entrez id written 21 hours ago by modarzi • 20
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