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convert SNP posiotions to VCF file
genome forum next-gen snp written 3 days ago by balathumma100 • updated 3 days ago by Goutham Atla6.7k
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Molecular weight, SPDBV tool
molecular weight spdbv tool written 25 days ago by ashamscsoft0 • updated 2 days ago by Ram11k
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203
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optimum statistical test to get significance level
rna-seq written 7 weeks ago by ashkan60 • updated 11 days ago by Biostar ♦♦ 10
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about dali webserver
alignment written 28 days ago by contact.kalpanasingh0
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3
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162
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44
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4.6k
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22 follow
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Tutorial: List Of Bioinformatics Books
bioinformatics tutorial books written 3.7 years ago by Medhat6.0k
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118
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123
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Merge/Collapse regions within a certain distance
bedtools written 4 days ago by Adrian Pelin1.9k • updated 4 days ago by Pierre Lindenbaum88k
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219
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Repeatmasker Annotation Descriptions
repeatmasker ucsc written 25 days ago by morovatunc280 • updated 15 days ago by Biostar ♦♦ 10
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A Grep For Gene Ontology ?
gene filter written 6.8 years ago by Pierre Lindenbaum88k • updated 15 hours ago by Biostar ♦♦ 10
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Help Needed with Pbalign SamFIlter
quiver pbalign pacbio samfilter written 6 weeks ago by anniiee90 • updated 27 days ago by Biostar ♦♦ 10
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News: Short Term Industrial Bioinformatics Training for life sciences
ngs news rna-seq written 10 days ago by sukhada0 • updated 10 days ago by Giovanni M Dall'Olio24k
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169
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2
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How to call genotype bases for all the samples?
vcf software error pyvcf snps gt written 13 days ago by kirannbishwa01220 • updated 8 days ago by Dan Gaston6.5k
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6 follow
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Removing PCR duplicates from .fastq without .bam alignment
illumina fastq pcr duplicates written 2.1 years ago by Adrian Pelin1.9k • updated 1 day ago by Brian Bushnell8.8k
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174
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7 follow
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best criteria to find DE genes in RNA-seq analysis
p-value rna-seq adjusted p-value written 17 days ago by hougiotaejut10 • updated 17 days ago by Devon Ryan60k
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