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<prev • 28,824 results • page 1 of 961 • next >
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Creating a stable batch-corrected scRNA-Seq data with multiple datasets and multiple integrations
scrna-seq batch correction rna-seq written 1 minute ago by hkarakurt • 100
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CNVkit intervarls questions
cnvkit written 36 minutes ago by emmanouil.a • 20
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Regarding Barley genome
gene assembly genome written 1 hour ago by umeshtanwar2 • 20
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problem use htseq-count in bash script
htseq-count script written 2 hours ago by o.omidan • 0
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14
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Problem loading data from metadata file on Cytoscape
cytoscape written 2 hours ago by Eve.Roxborough • 0
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how to calculate TMB from call stats file
mutations written 2 hours ago by rotemkat • 0
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Comparative Genome Analysis vs. Comparative Genomics
comparativegenomeanalysis comparativegenomics written 2 hours ago by peifei0418 • 0
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How to obtain unspliced tRNAs from FASTQ file
next-gen rna-seq unspliced trna written 2 hours ago by nkabo • 50
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Sort Sam file by chromosome and position in python
genome python alignment sam written 3 hours ago by hectorbaigessanchez • 0
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28
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what is the meaning of "consensus mutation"?
sequence sequencing written 3 hours ago by 2001linana • 10
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How to download TCGA normal sample ?
R tcga rna-seq written 4 hours ago by najioumayma • 10
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100
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How does FastQTL deal with strand
qtl rna-seq written 9 weeks ago by Cindy • 10 • updated 4 hours ago by Biostar ♦♦ 20
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Is there a reason for less IgG occupancy around the promoters of highly expressed genes?
igg chip-seq written 4 hours ago by jparker4 • 20
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94
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RNA seq analysis ( pre-processing)
R rna-seq written 4 days ago by najioumayma • 10
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22
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Determine heterozygosity with GenomeScope
genomescope heterozygosity written 5 hours ago by pablo • 150
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Why might a large number of variants fail HWE?
genome rna-seq snp written 6 days ago by srmeetd • 0 • updated 6 hours ago by i.sudbery ♦ 9.7k
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Question about Penncnv software
penncnv cnv written 7 hours ago by zkafi1370 • 0
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65
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Create files in multiple directories via for loop
shell linux written 8 hours ago by vinayjrao • 180
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33
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SnpSift case control command for multiple samples
snpsift casecontrol next-gen snp rna-seq written 8 hours ago by kumari.indu31 • 0
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25
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convenient VCF comparison
sequencing written 8 hours ago by storm1907 • 0
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How Can I plot this data in a heatmap?
R heatmap uniprot pathways written 9 hours ago by sharmatina189059 • 40
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analysis of gvcf file
snp written 10 hours ago by wongzlll • 0
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Which Regression Methods Are Suitable For Binary Valued Features And Continuous Output ?
statistics written 7.6 years ago by khan • 100 • updated 10 hours ago by Biostar ♦♦ 20
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Unknown X in amino acid sequences, creating error in epitope conservation study
sequence epitope prediction epitope conservation written 10 hours ago by anolidinasha • 0
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Intronic Variants in HGSVC notation
genome gene sequencing dna written 10 hours ago by biogirl04 • 10
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101
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Invitation to submit book chapter for spinger book
book chapter invitation written 1 day ago by manojevodevo • 30
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28
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How do you add up the results from two barcodes in an anndata object?
scrna-seq anndata written 15 hours ago by pomodoro_sinensis • 0
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33
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Impact of RNAseq read length on non-reference genome alignment
alignment rna-seq written 16 hours ago by rependo • 10
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what is the effective population size in a plot from psmc software?
gene psmc demography genome bioinformatics written 19 hours ago by a4appy23 • 10
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How to generate an ancestry test from 23andme genotyping data
ancestry written 19 hours ago by itlalcocaro • 0
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