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Tool: Circle-Map: Sensitive detection of circular DNA at single-nucleotide resolution using guided realignment of partially aligned reads
ecdna circdna tool eccdna written 8 months ago by IP • 620 • updated 3 minutes ago by berry • 10
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METAL (gwas meta-analysis tool)
gwas metal meta-analysis genomics bioinformatics written 23 hours ago by bigfoot • 0
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Protein contact map prediction machine learning approach
sequence written 11 minutes ago by akilaramu1998 • 0
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Z score and FC
rna-seq written 14 minutes ago by kanwarjag • 1.0k
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11
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Problems with using Phobius
genome software error sequence fasta phobius written 1 hour ago by logleg92029 • 0 • updated 24 minutes ago by h.mon ♦ 29k
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Theoretical question regarding trancriptomics
genome sequence rna-seq transcriptomics written 36 minutes ago by K.Gee • 20
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Job: Postdoctoral Fellow - Bioinformatician with experience in biological data analysis
biology job vacancy bioinformatician written 1 hour ago by EMBL Recruitment • 20
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Getting external ids with Bio.KEGG.REST
ensembl kegg written 1 hour ago by laalice3 • 0
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5 follow
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How to concatenate four fastq files of NextSeq in linux?
software error assembly alignment rna-seq genome written 3 days ago by harshraje19 • 10
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Problem with ks_debruijn4 on large dataset in KisSplice
software error rna-seq kissplice written 4 months ago by david.b.rombaut • 0
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Job: Genomic Data Analysis - Bioinformatician
biology data analysis job vacancy bioinformatician written 1 hour ago by EMBL Recruitment • 20
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BlastX Database: output search is empty
blastx database search error written 1 hour ago by marongiu.luigi • 450
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Downsampling UMI reads
umi next-gen rna-seq written 2 days ago by Bedirhan • 0
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BWA MEM using snakemake
snakemake bwa written 2 hours ago by User000 • 270
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scRNA samples: merge vs. integration
scrna single cell written 2 hours ago by jhb80 • 40
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News: The Biostar Handbook. A bioinformatics e-book for beginners.
tutorial news training handbook written 3.1 years ago by Istvan Albert ♦♦ 82k
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Remove sequence by coordinates with Biopython
fasta biopython written 3 hours ago by Darill • 40
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49
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1
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TaxID to RefSeq
genome ncbi written 3 hours ago by zuzanna.karwowska • 10
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allow mismatch in miRDeep2
mirdeep2 mismatch written 3 hours ago by anthihongthuy • 0
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pysamstats produces 'inaccurate' variants frequencies?
snp written 3 hours ago by Lhl • 730
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49
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How to retrieve from a GFF3 file a AA and CDS files
gene annotation written 5 hours ago by Ric • 290 • updated 3 hours ago by Juke-34 • 3.3k
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refRANK error: Assembly_genomic.fna contains multiple FASTA entries
software error written 3 hours ago by smccarthy1995 • 0
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Allele Frequency Thershold
1000g allele frequency annovar written 3.7 years ago by 786 • 50 • updated 3 hours ago by Biostar ♦♦ 20
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Interested in RNA-Seq splicing analysis - go for paired-end shorter or single-end longer?
splicing rna-seq sequencing written 4 hours ago by brown.annaleigh • 0 • updated 4 hours ago by ATpoint ♦ 28k
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Visualizing pedigrees from Plink files
pedigree plink plot written 7.1 years ago by alexhli • 80 • updated 4 hours ago by zx8754 ♦ 8.9k
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(Closed) how can i find differentailly expressed genes between two data set?
R genes differentialy expressed rna-seq written 5 hours ago by husainbioinfos • 0
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244
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changing ID in an existing GFF3 file
gene annotation written 7 weeks ago by Ric • 290 • updated 4 hours ago by lieven.sterck ♦ 6.8k
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how to get RNA-binding proteins in mouse
clip-seq proteomics chip-seq rna-seq written 4 hours ago by ta_awwad • 240
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Interpretation of hazard ratio
hazard ratio survival analysis hr written 9 hours ago by huynguyen96.dnu • 10
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Any changes to the frequencies of gnomAD v2.1 liftover ?
hg38 gnomad liftovert hg19 written 1 day ago by badredda • 120
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