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<prev • 4,950 results • page 1 of 165 • next >
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Species variation after longer sequencing time
assembly next-gen sequencing written 4 hours ago by firminlago • 0
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1
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55
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1
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Are there advantages in using high accuracy models for guppy basecaller when Illumina data are available?
genome assembly sequencing written 18 hours ago by ikangkim • 30 • updated 8 hours ago by colindaven • 1.9k
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Job: Do you want to have notable impact on how Statens Serum Institut works with viral Next Generation Sequencing (NGS) data for surveillance?
virology ngs job sequencing written 8 hours ago by info • 0
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1
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38
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1
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How to use ExAC/gnomAD without chrN_random?
variant calling exac snp sequencing written 9 hours ago by dodausp • 120 • updated 9 hours ago by Pierre Lindenbaum ♦ 124k
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how to interpret NextSV Sniffles 0/0 genotype ?
assembly alignment sequencing written 14 hours ago by blazyte.asta • 0
2
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112
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Creating BWA index files from custom fasta file
genome alignment rna-seq sequencing written 1 day ago by robbertijsselsteijn • 0 • updated 1 day ago by genomax ♦ 75k
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1
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54
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1
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Fusion orientation make sense or not
gene sequence next-gen sequencing written 3 days ago by 9521ljh • 10 • updated 1 day ago by trausch • 1.4k
2
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1
answer
77
views
1
answer
ERROR in sam to bam conversion
rna-seq sequencing written 6 days ago by antoromitelli • 10
3
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1
answer
829
views
1
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Crispr-cas9 screen analysis mageck
crispr-cas9 mageck sequencing written 21 months ago by 11yj3312 • 0 • updated 1 day ago by dsull • 630
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61
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ctDNA WES duplication rates from NovaSeq 6000 and HiSeq 4000
novaseq illumina wes sequencing written 2 days ago by graeme.thorn • 40
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1
answer
98
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1
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Whole Exome Sequencing analysis pipeline
sequencing written 3 days ago by Rick P • 10 • updated 2 days ago by Kevin Blighe ♦ 52k
3
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1
answer
80
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1
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Barcode Fastq Header - Adding Characters
sequencing written 3 days ago by zach • 0
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0
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48
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Nanopore hybrid assembly
next-gen nanopore sequencing written 2 days ago by ma23 • 40
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49
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ChIP-seq lack of nucleosome depleted region
genome assembly chip-seq sequencing written 2 days ago by bweekley • 0
2
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2
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106
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2
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Definition of an isoform switching?
gene genome rna-seq sequencing written 3 days ago by a4appy23 • 10 • updated 3 days ago by b.bearmi • 0
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59
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Error in PGAP pangenome pipeline?
genome gene sequence bioinformatics sequencing written 3 days ago by Dineshkumar K • 30
0
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1
answer
273
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1
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Chromatin Features Database?
genome sequencing written 17 months ago by mattysi • 0 • updated 4 days ago by rishi • 10
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2
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65
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2
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How to extract features from protein sequence for classification
gene sequence sequencing written 4 days ago by lacolombemarouane • 0 • updated 4 days ago by skjobs0123 • 50
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0
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75
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How to view gi_taxid_nucl.dmp that is 11.3 GB from NCBI
sequence sequencing written 4 days ago by peggyw • 0
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90
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Switch ref/alt alleles vcf file
vcf snp sequencing written 6 days ago by mdstep • 0
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0
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106
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Single Cell RNA-Seq : Should I trim Poly-T & Clontech sequences called as "Overrepresented sequences" by FastQC ?
next-gen rna-seq sequencing written 7 days ago by gsr9999 • 120 • updated 7 days ago by genomax ♦ 75k
4
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1
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111
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1
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What is the difference between paired end reads and overlapping reads, and then why merge overlapping reads before assembly?
genome assembly sequencing written 7 days ago by robert.murphy • 0 • updated 7 days ago by lieven.sterck ♦ 6.4k
1
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1
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92
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1
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Technical challenges inherent to WES processing - any recommended review sources?
next-gen wes sequencing written 7 days ago by asg • 0 • updated 7 days ago by Nicolas Rosewick ♦ 8.5k
1
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112
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Low BUSCO completeness value for protists
assembly next-gen sequencing written 8 days ago by qingtian.guan • 0 • updated 8 days ago by genomax ♦ 75k
7
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1
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11k
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1
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Help understanding the non-coding exons in a gene.
gene sequencing written 5.1 years ago by Affan • 290 • updated 10 days ago by Biostar ♦♦ 20
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1
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149
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1
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nanopor reads analysis using nanoplot
software error sequencing written 12 days ago by firminlago • 0 • updated 10 days ago by lieven.sterck ♦ 6.4k
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1
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120
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1
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How to extract a specific gene sequence for a specific cell from scRNA-seq fastq file
scrna-seq sequencing written 12 days ago by cook.675 • 10 • updated 11 days ago by mahmoud.s.fahmy • 0
2
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2
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141
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2
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Extract samples from a bcf files based on genotype?
genome next-gen snp sequencing written 12 days ago by ste.lu • 50 • updated 12 days ago by chrchang523 ♦ 6.2k
1
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116
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Explanation for SNP data and its relativeness to the allele frequency
genome R next-gen snp sequencing written 12 days ago by albertoogy • 0 • updated 12 days ago by Joe ♦ 15k
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128
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1
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Which is the best dna kit in the us market
snp sequencing written 12 days ago by abuzarhamza • 0 • updated 12 days ago by Charles Warden ♦ 7.5k
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