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<prev • 670 results • page 1 of 23 • next >
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adding pair info to fastq files, for BWA
illumina bwa sra written 6 days ago by sullis02 • 0
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57
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local assembly, how to proceed?
rad-seq illumina written 5 days ago by gbl1 • 70
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Is there any other options to fetch the rs-ids for the markers for the Illumina custom array?
illumina iscan dbsnp snp rsids written 13 days ago by bioinforesearchquestions • 200
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Illumina genotyping report to Plink files
illumina snp plink conversion written 4.1 years ago by egustavsson • 10 • updated 17 days ago by Phoenix Mu • 0
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Handling Illumina Omni2.5 data from multiple array versions and multiple genome version (with a view for CNV calling)
illumina snp penncnv omni2.5 written 4.6 years ago by Nicholas Blackburn • 90 • updated 17 days ago by michau • 10
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146
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Problem with demultiplexing illumina dual indexed libraries
illumina next-gen sequence rna-seq sequencing written 18 days ago by sikhtechai • 30 • updated 18 days ago by Gabriel R. • 2.6k
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144
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Are the Fastq files content is truly random
illumina fastq hiseq written 20 days ago by yonis • 0 • updated 20 days ago by Istvan Albert ♦♦ 80k
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Many 35nt reads with N bases in R1(paired-end) when sequencing with Illumina NextSeq
illumina rna-seq qualitycontrol written 20 days ago by mgdrnl • 10 • updated 20 days ago by Nicolas Rosewick ♦ 7.5k
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illumina results to do genotype imputation,about AB to ATCG
illumina snp genotype imputation written 2.7 years ago by sacuba1 • 0 • updated 4 weeks ago by mw955 • 0
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74
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RadSeq and short read
illumina radseq clustering written 5 weeks ago by gbl1 • 70
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6 follow
3
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bcl2fastq2: how to correctly use the --use-bases-mask for different sequencing methods by Illumina ?
illumina --use-bases-mask bcl2fastq2 sequencing written 6 months ago by badredda • 90
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2
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123
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masurca runCA failed
masurca assembly tool stack illumina written 6 weeks ago by mariachiaracascarano • 10
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different extractions for Hybrid assembly
illumina hybrid assembly dna extraction minon written 6 weeks ago by mariachiaracascarano • 10
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Blog: NGS-based research, empowering medical professionals through user-friendly software
illumina ngs dna-seq blog diagnostics written 8 weeks ago by David Langenberger ♦ 8.7k
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132
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How to take out sequences with barcode?
illumina fastq sequencing barcode written 7 weeks ago by suvratha • 20 • updated 7 weeks ago by Ido Tamir ♦ 5.0k
2
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2
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144
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2
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masurca invalid forward file for PE library
assembly tool masurca illumina written 7 weeks ago by mariachiaracascarano • 10
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1
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129
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1
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De novo transcriptome assembly using Trinity
gaiix illumina rna-seq written 8 weeks ago by 1234anjalianjali1234 • 30 • updated 8 weeks ago by JC ♦ 7.7k
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1
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875
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How To Remap Humanht V4 Chips To Hg19?
illumina microarray written 5.1 years ago by liu4gre • 200 • updated 10 weeks ago by Biostar ♦♦ 20
2
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1
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166
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1
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Is there a benefict of denoising reads for project that are not using 16S amplicon ?
illumina 16s denoising amplicon written 11 weeks ago by sacha • 1.7k • updated 11 weeks ago by Asaf ♦ 5.5k
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1
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249
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1
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within array vs between array normalization (methylation)
normalization methylation microarrays illumina written 12 weeks ago by rorio • 10 • updated 12 weeks ago by Kevin Blighe ♦ 41k
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1
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246
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1
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Number of passing clusters vs. number of read pairs vs. total number of reads
reads illumina flowcell written 3 months ago by AP • 90 • updated 3 months ago by genomax ♦ 65k
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237
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Assembling ESTs and illumina reads
ests illumina de-novo transcriptome written 3 months ago by Joseph Hughes • 2.7k
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3
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464
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6 follow
3
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add UMI sequences to fastq read name
illumina umi fastq written 3 months ago by User6891 • 250 • updated 3 months ago by i.sudbery ♦ 4.3k
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1
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240
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1
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Extracting contaminated reads from the sequenced data
genome illumina extraction sequencing written 3 months ago by manjumoorthy95 • 0 • updated 3 months ago by genomax ♦ 65k
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204
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1
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PhiX forward and reverse reads for MiSeq and NextSeq Platform
illumina next-gen sequencing written 3 months ago by kspata • 40
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1
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212
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1
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Best way of Merging Multiple Lanes generated by HiSeq 2000, index BAM or VCF?
wgs sam mapping illumina hiseq written 3 months ago by venuraherath • 20
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140
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Strain Assignments to QTL Data
qtl muga rqtl2 genotype illumina written 3 months ago by annacsalvador • 0
5
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280
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5 follow
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Merging fastq files
illumina fastq miseq merge rna-seq written 6 months ago by william.mcentegart • 0 • updated 3 months ago by Biostar ♦♦ 20
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176
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Meaning of TOP/BOTTOM strand and QC implications
illumina snp written 4 months ago by ognjen011 • 150
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Trio SNP data to test script (preferably from Infinium Global Screening Array)
trio array microarray snp illumina written 4 months ago by kurt.cagri • 0
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