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<prev • 81,097 results • page 1 of 2704 • next >
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removing decimal from ENSEMBL gene ID
genome R assembly written 3 minutes ago by asajesan04 • 0
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Ancestry inference cases-controls targeted NGS, small gene set
population structure pca ethnicity targeted ngs written 7 hours ago by nikimourtzi23 • 0 • updated 10 minutes ago by genomax ♦ 80k
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samr analysis: How to interpret Median FDR/90th perc FDR=0.000000?
microarray samr written 17 days ago by grd • 0 • updated 10 minutes ago by Biostar ♦♦ 20
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Exract variable protein sequence from multiple seqece alinment?
alignment tool written 56 minutes ago by mdshaminurrahman95 • 0 • updated 54 minutes ago by ATpoint ♦ 32k
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2
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52
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How reliable are the ensembl transcript isoforms?
ensembl rna-seq isoform written 15 hours ago by simplitia • 30 • updated 1 hour ago by vkkodali • 1.9k
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how to concetanate column values of a data frame and converting single letters of snp calls to bi allelic in R?
R snp written 1 hour ago by blacktomato27 • 50
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35
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StringTie output to train Augustus
gene annotation written 4 hours ago by Ric • 290
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58
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Visualisation of SNPcoverage genomewide
software snp written 1 day ago by steinfried12 • 0 • updated 6 hours ago by Biostar ♦♦ 20
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1
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38
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1
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How to convert ENSEMBL gene IDs to nucleotide sequences?
gene assembly sequence rna-seq sequencing written 9 hours ago by harshraje19 • 20 • updated 6 hours ago by Jean-Karim Heriche ♦ 21k
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1
answer
39
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Sort header from the multifasta sequnce file into only gene name
genome alignment sequence gene sequencing written 8 hours ago by k.kathirvel93 • 250 • updated 6 hours ago by gayachit • 170
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22
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232 follow
22
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News: The Biostar Handbook. A bioinformatics e-book for beginners.
tutorial news training handbook written 3.3 years ago by Istvan Albert ♦♦ 83k
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1
answer
67
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1
answer
Interpretation of SRA files
sra fastq paired-end reads headers written 15 hours ago by dominique.massau • 0 • updated 8 hours ago by wm • 350
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Infer CNV from ATAC-seq data
atac-seq cnv written 8 hours ago by BrunoGiotti • 110
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28
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How to get "best" taxon identifier from diamond output with staxids?
metagenomics alignment protein diamond blast written 9 hours ago by O.rka • 170
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1
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61
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1
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Genes Symbol Conversion not in biomaRt
gene rna-seq written 12 hours ago by bazok • 0
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35
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How do I know Seurat operates on what data? Raw count or scaled.data
rna-seq written 10 hours ago by 18982289189 • 0
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30
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HIV NL4-3 transcriptome fasta
clip-seq rna-seq written 11 hours ago by xiaoleiusc • 20
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63
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GATK's new best practice for mitochondrial variant calling
snp sequencing written 11 days ago by lovelysunzt • 0 • updated 12 hours ago by Biostar ♦♦ 20
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34
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snpEff: Single variants are double-counted in Ts/Tv summary
ti/tv ratio snpeff ts/tv ratio written 13 hours ago by kenyonalexander0 • 0
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51
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Applying QC on merged reads from illumina
genome illumina next-gen sequencing written 14 hours ago by Usama Bakry • 0 • updated 13 hours ago by Pierre Lindenbaum ♦ 127k
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2
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MD5 not the same between contig and reference; both Unified Genotyper and Haplotype Caller
vcf gatk md5 written 14 hours ago by j.lunger18 • 10 • updated 14 hours ago by igor ♦ 9.9k
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Measure genetic distance between populations (Fst value)
software error snp written 15 hours ago by jessicadorner • 0
1
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1
answer
64
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1
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Analyzing SortMeRNA extracted 16S rRNA
de novo assembly 16s sortmerna metagenomics written 16 hours ago by kmyers2 • 40 • updated 15 hours ago by h.mon ♦ 29k
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37
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Bedtools Fisher Genome File
bedtools genome fisher overlap chipseq written 15 hours ago by megannj • 10 • updated 15 hours ago by Pierre Lindenbaum ♦ 127k
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36
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Mapping reads to repetitive positions in reference within edit distance and with 1 indel
bbmap mapping bowtie written 16 hours ago by pawlowac • 70
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adding in new evidence to a Maker annotation job
annotation maker written 15 hours ago by devon.orourke • 10
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61
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1
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Find HBV integration sites in human genome.
chimericreads humanvirusgenome cage-seq written 16 hours ago by Chirag Nepal • 2.2k • updated 15 hours ago by Pierre Lindenbaum ♦ 127k
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36
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SRA file identifiers for use with sra-toolkit
sra-toolkit written 16 hours ago by ScubaChris • 10
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64
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SNP subsetting using bcftools
next-gen bcftools snp written 18 hours ago by alexcullsci • 0 • updated 17 hours ago by Kevin Blighe ♦ 56k
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Gene Cluster Detection
genome annotation alignment written 16 days ago by biohacker_tobe • 40 • updated 18 hours ago by Biostar ♦♦ 20
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