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Error using bwasw (bwa 0.7.15-r1140): bwtsw2_pair.c line 122: failed to allocate memory
alignment dna-seq bwa written 17 months ago by azaharamft • 0 • updated 15 hours ago by finswimmer ♦ 8.0k
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Get Flanking Amino Acid Sequence
R dna-seq sequence snp python written 11 days ago by windsur • 10
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5 follow
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News: [UPDATED] Hands-On NGS Data Analysis Workshops 2019
news dna-seq ngs bisulfite-seq rna-seq written 11 days ago by David Langenberger ♦ 8.4k
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143
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Forum: Survey - Tell me about your Bioinformatics struggles
forum dna-seq multiomics rna-seq computational biology written 23 days ago by p.hadjipanayiotou • 0 • updated 23 days ago by jrj.healey ♦ 9.1k
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Small DNA-seq read files for tests
dna-seq next-gen written 8 weeks ago by chefarov • 110
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Is the union of cDNA sequences the exome?
exome cdna dna-seq written 11 weeks ago by Bioaln • 290 • updated 11 weeks ago by lieven.sterck • 3.3k
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VELVET de novo plant genome, strategy question
dna-seq eucharyotes velvet written 2.8 years ago by dsoronellas • 20 • updated 11 weeks ago by RamRS ♦ 19k
13
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5 follow
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Paternity Testing from WGS Trio
trio wgs dna-seq paternity test written 3 months ago by ClkElf • 20 • updated 3 months ago by RamRS ♦ 19k
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samtools bedcov vs. bedtools coverage
dna-seq coverage written 2.5 years ago by Dataman • 260 • updated 3 months ago by RamRS ♦ 19k
8
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429
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7 follow
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Removing Duplicates before aligning
gatk dna-seq next-gen written 5 months ago by newbinf • 0 • updated 5 months ago by gb • 520
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[CNV] doubt with the results of cn.mops on different reference genomes
dna-seq sequence cnv written 5 months ago by dacacis • 0 • updated 5 months ago by pbpanigrahi • 180
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Removing Illumina Single End PCR Primers and TruSeq Adapters
adapter removal dna-seq primer truseq fastqc written 5 months ago by serpalma.v • 20 • updated 5 months ago by genomax ♦ 59k
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controls for amplicon data - Which one to use and how?
amplicon dna-seq control written 3.7 years ago by Aurelie MLB • 310 • updated 5 months ago by Biostar ♦♦ 20
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News: LAST CALL - 'Introduction to NGS Data Analysis' course in Berlin, October 8-10 2018
news dna-seq training ngs rna-seq written 6 months ago by David Langenberger ♦ 8.4k
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Extracting genotypes and filtering from a VCF file containing multiple exomes of families
vcf filter exome dna-seq genotype written 6 months ago by gradstudentNew • 10 • updated 6 months ago by Pierre Lindenbaum ♦ 115k
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Peak calling with MACS for paired end DNase-seq data
macs2 paired-end dna-seq bwa written 7 months ago by Bioinformatist Newbie • 230 • updated 7 months ago by igor ♦ 7.1k
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News: NCBI NOW (Next generation sequencing Online Workshop) October 13 - 23 , 2015
ncbi news mapping ngs rna-seq dna-seq written 3.2 years ago by rtliu • 2.0k • updated 7 months ago by f.hashemigorji • 0
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News: Webinar on Diagnosis of Rare Diseases using NGS Based Multi-gene Testing- Case studies by Dr.Aparna Ganapathy on 18 Apr 2018
variant calling news dna-seq strand ngs rare disease written 9 months ago by Genomics • 70
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How to do NGS Analysis of a Particular Gene?
gene dna-seq snp written 8 months ago by user5212 • 0 • updated 8 months ago by finswimmer ♦ 8.0k
3
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420
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GC Bias Correction
gc dna-seq written 8 months ago by finswimmer ♦ 8.0k
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418
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1
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News: 2nd Berlin Summer School in NGS Data Analysis 2018
news dna-seq ngs workshop rna-seq written 8 months ago by David Langenberger ♦ 8.4k • updated 8 months ago by Adele Feuerstein • 460
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genemark-es gene-finding with reference and annotation
assembly gene prediction dna-seq written 9 months ago by from the mountains • 40 • updated 9 months ago by lieven.sterck • 3.3k
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Is Paired End analysis possible with FASTQC?
paired-end dna-seq qc fastqc written 2.6 years ago by chefarov • 110 • updated 10 months ago by Stephane Plaisance • 380
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Is it possible to check whether a sample is progeny of the other two samples from exome sequenced data?
exome ngs dna-seq snp written 10 months ago by bioinforesearchquestions • 190 • updated 10 months ago by Noushin N • 530
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347
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heterozygosity during variant calling in a non-model organism such as Bubalus Bubalis
next-gen dna-seq snp sequencing written 10 months ago by prasundutta87 • 280
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Median coverage from BAM file
dna-seq coverage written 11 months ago by rmf • 460 • updated 11 months ago by Alex Reynolds ♦ 26k
2
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Mutations and copy number variations from DNA-Seq
cna dna-seq snp cnv sequencing written 11 months ago by ciemanek • 110 • updated 11 months ago by Amitm • 1.6k
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873
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Dealing with multiple read groups, from BWA to sorted .bam
dna-seq sequence written 11 months ago by jamiedm • 0
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418
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0
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Tool for Pathway Analysis on SKAT results
skat exome dna-seq pathway analysis written 12 months ago by anp375 • 140
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454
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Integrated DNA and RNA sequences in expression analysis
dna-seq rna-seq written 12 months ago by bwczech • 40 • updated 12 months ago by ori • 50
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