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<prev • 743 results • page 1 of 25 • next >
1
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48
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Multiple VCF filtering
vcf wgs exom illumina written 2 days ago by deniselavezzari • 0 • updated 2 days ago by RamRS ♦ 27k
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29
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0
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GenePattern: Where can I find IlluminaNormalizer module
illumina genepattern microarray normalization written 3 days ago by siltoon1 • 0
4
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2
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194
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2
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Illumina HumanHT-12 V3.0 expression beadchip reading data
illumina gene expression affy microarray written 4 months ago by bhargavdave1 • 0 • updated 6 days ago by zhijianzheng007 • 10
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1
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1
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Automating Paired End mating
assembly automation paired end illumina written 5.5 years ago by Furor • 40 • updated 7 days ago by Biostar ♦♦ 20
0
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150
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0
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PICARD ExactIlluminaBarcodes with NO BARCODES ILLUMINA LIBRARY
illumina picard bcl2fastq basecalling sequencing written 22 days ago by dishasharma35 • 0 • updated 22 days ago by RamRS ♦ 27k
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92
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Bimodal %GC plot of fastqc output in RNASeq
rice illumina rna-seq %gc fastqc written 4 weeks ago by devbt15 • 10 • updated 4 weeks ago by ATpoint ♦ 36k
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0
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101
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0
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splicing with UMI barcodes - paired end illumina sequencing
illumina umi umitools splicing star written 5 weeks ago by snishtala03 • 30
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0
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155
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0
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Convert illumina id to official gene symbol
gene illumina offiicial-gene-symbol written 7 weeks ago by donnieDarko • 0
0
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1
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167
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1
answer
RNA-seq Nanopore and Illumina hybrid assembly to improve gene annotation
illumina rna-seq nanopore assembly written 10 weeks ago by nlehmann • 90 • updated 9 weeks ago by colindaven • 2.3k
6
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2
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2.4k
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5 follow
2
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Bisulfite Analysis With Illumina Fastq From Different Lanes
illumina fastq next-gen sequencing written 8.5 years ago by Tonig • 440 • updated 9 weeks ago by iraia.munoa • 100
0
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0
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70
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0
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illumina variant interpreter vcf format version error
vcf illumina version written 9 weeks ago by SurdanBurasi • 0
0
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1
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303
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1
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Trim NEBnext Adapters with trimmomatic - Same as TruSeq adapters?
genome illumina quality check next-gen raw reads written 4 months ago by alexgoro13 • 0 • updated 9 weeks ago by ATpoint ♦ 36k
17
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5
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7 follow
5
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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 20 months ago by δΉ™ • 150 • updated 10 weeks ago by theodore • 60
2
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1
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155
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1
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Do illumina instruments generate four fastq files per sample?
illumina fasq lane written 11 weeks ago by DataFanatic • 230 • updated 11 weeks ago by genomax ♦ 85k
0
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0
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95
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How to annotate illumina HumanHT-12_V3_0_R3_11283641_A.txt data
genome illumina array written 11 weeks ago by a.james • 210
1
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1
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178
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6 follow
1
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free linux server
genome assembly illumina written 3 months ago by VSR • 0 • updated 12 weeks ago by colindaven • 2.3k
0
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0
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133
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0
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Applying QC on merged reads from illumina
genome illumina next-gen sequencing written 3 months ago by Usama Bakry • 0 • updated 3 months ago by Pierre Lindenbaum ♦ 129k
0
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1
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784
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1
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Error when changing the database for minfi dropLociWithSnps
methylationepic minfi illumina snp methylation written 3.0 years ago by Ellen O • 10 • updated 3 months ago by steffanchristiansen • 0
0
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0
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144
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0
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SRA run data access
ncbi sra next-gen sequence illumina written 3 months ago by DC7 • 20
5
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0
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218
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5 follow
0
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Analyze methylation microarray
genome methylation beadarray microarray illumina written 3 months ago by youseeisme • 0
1
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1
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227
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1
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Illuminate illuminate for NovaSeq
novaseq illumina next-gen interop written 8 months ago by pacman • 50 • updated 4 months ago by jfx319 • 10
0
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0
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148
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0
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Does Nextera Transposase adapter sequence affects GATK HaplotypeCaller pipeline?
gatk ngs snp rna-seq illumina written 4 months ago by Susmita Mandal • 60
0
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0
answers
151
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0
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Problem on mapping SNP ID
illumina snp written 4 months ago by cerriguglielmo • 0
2
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0
answers
127
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0
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Picard MarkDuplicates tool on a pooled sample BAM
illumina picard markduplicates written 4 months ago by joneill4x • 80
1
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1
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167
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1
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Multiple N bases in RNAseq
illumina rna-seq written 5 months ago by jgarces • 20
4
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1
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246
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5 follow
1
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Skewed beta-distribution from Methylation EPIC array data
metylation epic illumina champ written 5 months ago by erwin.tomasich • 0 • updated 5 months ago by Charles Warden ♦ 7.8k
0
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0
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229
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0
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Help with bowtie2 aligning PE Radseq sequences to reference genome
genome bowtie2 radseq mapping illumina written 5 months ago by imda • 10
3
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1
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169
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1
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How to report coverage at overlapping regions of paired-end reads?
illumina paired-end written 5 months ago by francois • 10 • updated 5 months ago by h.mon ♦ 30k
3
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1
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237
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1
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How to process data from Illumina sequencing ?
genome trimmomatic data illumina sequencing written 5 months ago by vicslab • 0 • updated 5 months ago by Michael Dondrup ♦ 47k
3
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2
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217
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2
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Example NGS data
illumina fastq next-gen cutadapt written 5 months ago by ksgajula • 0 • updated 5 months ago by devarora • 150
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