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Answer: A: Structural variation detection from RNA-seq
8.1 years ago by colindaven 8.1k
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3.5k
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Answer: A: Best Alignment tool of Denovo assembly Results.
8.1 years ago by colindaven 8.1k
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13k
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Comment: C: Any methods available to do QC analysis of Pacbio raw data??
8.1 years ago by colindaven 8.1k
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3.5k
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Answer: A: DiscovarDenovo - fastq files should be interlaced
8.2 years ago by colindaven 8.1k
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0
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1.9k
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Answer: A: How I get test group variants from multi-sample VCF of test group, control group
8.2 years ago by colindaven 8.1k
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2.6k
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Answer: A: Performing liftOver between genome assemblies not available on UCSC genome brows
8.2 years ago by colindaven 8.1k
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3.2k
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Comment: C: Improving existing assembly using PacBIo reads
8.2 years ago by colindaven 8.1k
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2.7k
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Answer: A: How can I Find modules of a gene?
8.2 years ago by colindaven 8.1k
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3.2k
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Answer: A: Improving existing assembly using PacBIo reads
8.2 years ago by colindaven 8.1k
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2.3k
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Comment: C: denovo pacbio assembly
8.2 years ago by colindaven 8.1k
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1
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1.8k
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Answer: A: why I got different number of peaks used differnt version reference of hexaploid
8.2 years ago by colindaven 8.1k
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0
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2.1k
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Answer: A: Assembly and annotation statistics collection of various eukaryote genomes
8.2 years ago by colindaven 8.1k
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0
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4.6k
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Comment: C: Variant annotation and filtration server ALAPY Genome Explorer (AGx)
8.2 years ago by colindaven 8.1k
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0
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4.8k
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Answer: A: Question: Normalization of read counts for Metagenomics data
8.2 years ago by colindaven 8.1k
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2.3k
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Answer: A: denovo pacbio assembly
8.2 years ago by colindaven 8.1k
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0
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1.8k
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Comment: C: SNPs detection in transcriptomics to define genetic variation between individual
8.2 years ago by colindaven 8.1k
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0
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1.8k
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Answer: A: SNPs detection in transcriptomics to define genetic variation between individual
8.2 years ago by colindaven 8.1k
1
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0
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3.5k
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Comment: C: How to delete everything after a certain point in GFF3 file - PYTHON
8.2 years ago by colindaven 8.1k
0
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1
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1.9k
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Comment: C: The novoBreak does not work well. Error : region "chr1:66670169-66671169" specif
8.3 years ago by colindaven 8.1k
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0
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3.8k
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Answer: A: NCI-60 RNA-seq data
8.3 years ago by colindaven 8.1k
1
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0
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1.8k
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Answer: A: randfold - problem with installation
8.3 years ago by colindaven 8.1k
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0
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1.8k
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Answer: A: From the revered Tuxedo Suite for NGS data analysis, under what circumstances co
8.3 years ago by colindaven 8.1k
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0
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2.8k
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Answer: A: how to include insertion and deletion in the consensus sequence from BWA referen
8.3 years ago by colindaven 8.1k
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0
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1.8k
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Answer: A: Tools and parameters for reference assisted eukaryotic genome assembly using a d
8.3 years ago by colindaven 8.1k
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0
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1.6k
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Answer: A: Variant calling in phased assemblies
8.3 years ago by colindaven 8.1k
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0
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1.5k
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Answer: A: What platform similar to Galaxy can handle multiple batch processing of bacteria
8.3 years ago by colindaven 8.1k
1
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0
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3.9k
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Answer: A: number of threads for cufflinks transcript assembly
8.3 years ago by colindaven 8.1k
0
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1
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1.8k
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Answer: A: Weird fragments when aligning PE reads to duplicated genes.
8.3 years ago by colindaven 8.1k
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0
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2.4k
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Comment: C: How to annotate novel SNPs using coding sequence position?
8.3 years ago by colindaven 8.1k
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0
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1.6k
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Answer: A: Using long reads to find a combination of mutations
8.3 years ago by colindaven 8.1k
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0
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2.4k
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Answer: A: How to annotate novel SNPs using coding sequence position?
8.3 years ago by colindaven 8.1k
0
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0
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3.3k
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Answer: A: Functional annotation pipeline
8.3 years ago by colindaven 8.1k
1
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1
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2.6k
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Answer: A: if i do mistake in library type parameter of trinity assembly, do i need to reas
8.3 years ago by colindaven 8.1k
1
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0
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3.7k
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Comment: C: SNPs Calling Tools
8.4 years ago by colindaven 8.1k
1
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2
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3.0k
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Forum: bbmap callvariants.sh on pacbio
SNP
updated 2.8 years ago by 45k • written 8.4 years ago by 8.1k
0
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1
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2.6k
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Comment: C: if i do mistake in library type parameter of trinity assembly, do i need to reas
8.4 years ago by colindaven 8.1k
1
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1
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2.6k
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Comment: C: if i do mistake in library type parameter of trinity assembly, do i need to reas
8.4 years ago by colindaven 8.1k
0
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1
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3.7k
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Comment: C: SNPs Calling Tools
8.4 years ago by colindaven 8.1k
0
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1
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3.7k
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Answer: A: SNPs Calling Tools
8.4 years ago by colindaven 8.1k
3
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1
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2.0k
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Answer: A: STAR Indexing problems with unassambled vertebrate genomes
8.4 years ago by colindaven 8.1k
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0
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2.8k
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Answer: A: How to plot SNPs along a chromosome?
8.5 years ago by colindaven 8.1k
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0
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1.5k
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Answer: A: Finding HTSeq count data for NIH datasets.
8.5 years ago by colindaven 8.1k
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0
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2.9k
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Answer: A: Finding reference SNP ID numbers from Chrom POS in VCF of my Exome
8.8 years ago by colindaven 8.1k
5
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2.8k
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Answer: A: Gene annotation pipeline for bacteria
8.8 years ago by colindaven 8.1k
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0
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1.8k
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Comment: C: Processing SOLiD data but cannot find relevant documentation on tools (BFAST)
8.9 years ago by colindaven 8.1k
1
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1
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1.8k
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Answer: A: Processing SOLiD data but cannot find relevant documentation on tools (BFAST)
9.0 years ago by colindaven 8.1k
4
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0
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29k
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Answer: A: Best way to compare two samples in a VCF file
9.0 years ago by colindaven 8.1k
0
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1
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4.5k
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Answer: A: How to differentiate between prokaryotic and eukaryotic transcript from RNAseq d
9.0 years ago by colindaven 8.1k
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0
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2.5k
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Answer: A: scaffold in reference genome
9.0 years ago by colindaven 8.1k
0
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0
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2.5k
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Answer: A: please share your experience for ORF prediction +blastp instead of doing blastx
9.0 years ago by colindaven 8.1k
1,118 results • Page 22 of 23
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