Profile Posts Awards
Show
all questions tools blogs news tutorials forum answers comments
Showing : comments
0
votes
1
reply
9.1k
views
Comment: C: Should I consider contigs.fa or scaffolds.fa from SPAdes output for downstream a
5.9 years ago by bioinforesearchquestions ▴ 370
0
votes
1
reply
9.1k
views
Comment: C: Should I consider contigs.fa or scaffolds.fa from SPAdes output for downstream a
5.9 years ago by bioinforesearchquestions ▴ 370
0
votes
1
reply
9.1k
views
Comment: C: Should I consider contigs.fa or scaffolds.fa from SPAdes output for downstream a
5.9 years ago by bioinforesearchquestions ▴ 370
0
votes
0
replies
3.0k
views
Comment: C: Kmer selection for bacterial WGS denovo assembly using SPAdes or SOAP-denovo
5.9 years ago by bioinforesearchquestions ▴ 370
0
votes
1
reply
3.0k
views
Comment: C: Kmer selection for bacterial WGS denovo assembly using SPAdes or SOAP-denovo
6.0 years ago by bioinforesearchquestions ▴ 370
0
votes
1
reply
3.0k
views
Comment: C: Kmer selection for bacterial WGS denovo assembly using SPAdes or SOAP-denovo
6.0 years ago by bioinforesearchquestions ▴ 370
0
votes
1
reply
2.4k
views
Comment: C: How to find pathogenicity of a single missense variant ?
6.1 years ago by bioinforesearchquestions ▴ 370
1
vote
0
replies
2.4k
views
Comment: C: How to find pathogenicity of a single missense variant ?
6.1 years ago by bioinforesearchquestions ▴ 370
0
votes
1
reply
2.4k
views
Comment: C: How to find pathogenicity of a single missense variant ?
updated 6.1 years ago by 151k • written 6.1 years ago by ▴ 370
0
votes
1
reply
1.7k
views
Comment: C: Selecting methods for performing pairwise RNAseq analysis without replicates
6.3 years ago by bioinforesearchquestions ▴ 370
0
votes
1
reply
1.7k
views
Comment: C: Selecting methods for performing pairwise RNAseq analysis without replicates
6.3 years ago by bioinforesearchquestions ▴ 370
0
votes
1
reply
1.7k
views
Comment: C: Selecting methods for performing pairwise RNAseq analysis without replicates
6.3 years ago by bioinforesearchquestions ▴ 370
0
votes
0
replies
1.3k
views
Comment: C: Identifying consensus sequence between multiple Arabidopsis genome sequences
6.4 years ago by bioinforesearchquestions ▴ 370
0
votes
0
replies
3.5k
views
Comment: C: Pathway analysis and Gene enrichment Analysis Queries
6.5 years ago by bioinforesearchquestions ▴ 370
0
votes
1
reply
3.5k
views
Comment: C: Pathway analysis and Gene enrichment Analysis Queries
6.5 years ago by bioinforesearchquestions ▴ 370
0
votes
0
replies
1.9k
views
Comment: C: mirdeep2 v 10
updated 6.5 years ago by 45k • written 6.5 years ago by ▴ 370
0
votes
0
replies
2.3k
views
Comment: C: cummeRbund create database ERROR
6.5 years ago by bioinforesearchquestions ▴ 370
0
votes
0
replies
1.9k
views
Comment: C: Error in cummeRbund R library package (Error: Columns index not found)
6.5 years ago by bioinforesearchquestions ▴ 370
0
votes
1
reply
1.9k
views
Comment: C: Error in cummeRbund R library package (Error: Columns index not found)
6.6 years ago by bioinforesearchquestions ▴ 370
0
votes
0
replies
2.5k
views
Comment: C: I have some queries on coverage
updated 6.7 years ago by 45k • written 9.2 years ago by ▴ 370
0
votes
1
reply
5.9k
views
Comment: C: What is the appropriate assembler for PacBio long reads
6.8 years ago by bioinforesearchquestions ▴ 370
0
votes
0
replies
2.1k
views
Comment: C: Need help in selecting the correct output file from miRDeep2?
7.1 years ago by bioinforesearchquestions ▴ 370
0
votes
0
replies
3.8k
views
Comment: C: How to anntate small-RNA seq reads distribution
7.1 years ago by bioinforesearchquestions ▴ 370
0
votes
0
replies
2.2k
views
Comment: C: What are the methods to downsample the Depth of coverage (ex: 50X -> 25X)?
7.1 years ago by bioinforesearchquestions ▴ 370
0
votes
0
replies
3.9k
views
Comment: C: How to create bigwig using mm10.fasta and mm10.fasta bowtie index files
7.2 years ago by bioinforesearchquestions ▴ 370
0
votes
0
replies
1.9k
views
Comment: C: Need tools recommendation for plant RNAseq data
7.3 years ago by bioinforesearchquestions ▴ 370
0
votes
1
reply
5.2k
views
Comment: C: How to validate the SNP calling pipeline?
7.3 years ago by bioinforesearchquestions ▴ 370
0
votes
0
replies
5.2k
views
Comment: C: How to validate the SNP calling pipeline?
7.3 years ago by bioinforesearchquestions ▴ 370
0
votes
0
replies
5.2k
views
Comment: C: How to validate the SNP calling pipeline?
7.3 years ago by bioinforesearchquestions ▴ 370
0
votes
0
replies
5.2k
views
Comment: C: How to validate the SNP calling pipeline?
7.3 years ago by bioinforesearchquestions ▴ 370
0
votes
0
replies
5.2k
views
Comment: C: How to validate the SNP calling pipeline?
7.3 years ago by bioinforesearchquestions ▴ 370
0
votes
1
reply
3.2k
views
Comment: C: How to generate FASTA sequence of genes and phylogenetic analysis from NGS seque
7.3 years ago by bioinforesearchquestions ▴ 370
0
votes
1
reply
3.2k
views
Comment: C: How to generate FASTA sequence of genes and phylogenetic analysis from NGS seque
7.4 years ago by bioinforesearchquestions ▴ 370
0
votes
1
reply
3.2k
views
Comment: C: How to generate FASTA sequence of genes and phylogenetic analysis from NGS seque
7.4 years ago by bioinforesearchquestions ▴ 370
0
votes
0
replies
4.6k
views
Comment: C: Do I need to provide the Illumina's target region bed file for qualimap?
7.4 years ago by bioinforesearchquestions ▴ 370
0
votes
1
reply
3.2k
views
Comment: C: How to generate FASTA sequence of genes and phylogenetic analysis from NGS seque
7.4 years ago by bioinforesearchquestions ▴ 370
0
votes
0
replies
3.8k
views
Comment: C: identification of viral gene from fastq or BAM file
7.4 years ago by bioinforesearchquestions ▴ 370
0
votes
1
reply
3.2k
views
Comment: C: How to generate FASTA sequence of genes and phylogenetic analysis from NGS seque
7.4 years ago by bioinforesearchquestions ▴ 370
0
votes
1
reply
3.2k
views
Comment: C: How to generate FASTA sequence of genes and phylogenetic analysis from NGS seque
7.4 years ago by bioinforesearchquestions ▴ 370
0
votes
0
replies
3.5k
views
Comment: C: uniqueome mappability file for EXCAVATOR-tool
7.5 years ago by bioinforesearchquestions ▴ 370
0
votes
1
reply
2.8k
views
Comment: C: Looking for wig base coverage file for hg19
7.5 years ago by bioinforesearchquestions ▴ 370
0
votes
0
replies
2.2k
views
Comment: C: Can I merge the exome interval lists from two different kits for identifying CNV
7.5 years ago by bioinforesearchquestions ▴ 370
1
vote
0
replies
3.2k
views
Comment: C: Help required for Bacterial RNAseq data
7.6 years ago by bioinforesearchquestions ▴ 370
0
votes
2
replies
3.5k
views
Comment: C: How come the QC-passed reads from samtools flagstat is different from FASTQ (R1+
7.6 years ago by bioinforesearchquestions ▴ 370
0
votes
0
replies
3.6k
views
Comment: C: What is the difference between log2(Mutant/Wildtype) or log2(Wildtype/Mutant) fr
7.6 years ago by bioinforesearchquestions ▴ 370
0
votes
1
reply
3.6k
views
Comment: C: What is the difference between log2(Mutant/Wildtype) or log2(Wildtype/Mutant) fr
7.6 years ago by bioinforesearchquestions ▴ 370
0
votes
2
replies
3.6k
views
Comment: C: What is the difference between log2(Mutant/Wildtype) or log2(Wildtype/Mutant) fr
7.6 years ago by bioinforesearchquestions ▴ 370
0
votes
0
replies
3.6k
views
Comment: C: What is the difference between log2(Mutant/Wildtype) or log2(Wildtype/Mutant) fr
7.6 years ago by bioinforesearchquestions ▴ 370
1
vote
0
replies
3.6k
views
Comment: C: What is the difference between log2(Mutant/Wildtype) or log2(Wildtype/Mutant) fr
7.6 years ago by bioinforesearchquestions ▴ 370
0
votes
2
replies
3.6k
views
Comment: C: What is the difference between log2(Mutant/Wildtype) or log2(Wildtype/Mutant) fr
7.6 years ago by bioinforesearchquestions ▴ 370
188 results • Page 2 of 4
Content Search
Users
Tags
Badges
Help About
FAQ
Access RSS
API
Stats

Use of this site constitutes acceptance of our User Agreement and Privacy Policy.

Powered by the version 2.3.6