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1.2k
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Comment: C: To get correlation of different ChIP-seq samples
5.2 years ago by colindaven 8.0k
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2.3k
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Comment: C: Annotation of non model fish (mahi mahi) genome
5.2 years ago by colindaven 8.0k
1
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0
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1.2k
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Answer: A: Eukaryotic Genome Annotation for a non-model organism
5.2 years ago by colindaven 8.0k
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1
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3.1k
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Comment: C: NCBI wants to remove quality scores from SRA
5.2 years ago by colindaven 8.0k
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0
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1.1k
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Answer: A: Assessing collapsed assembly ?
5.3 years ago by colindaven 8.0k
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1
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735
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Answer: A: Filtering microbial variants
5.3 years ago by colindaven 8.0k
1
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0
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9.0k
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Answer: A: Variant calling on Nanopore reads
5.3 years ago by colindaven 8.0k
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0
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1.8k
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Comment: C: Creating a bed file from a de novo fasta file
5.3 years ago by colindaven 8.0k
1
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0
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1.7k
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Answer: A: Removing UniVec sequences in Assembly
5.3 years ago by colindaven 8.0k
0
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0
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6.2k
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Answer: A: calculating abundance of metagenomes
5.3 years ago by colindaven 8.0k
0
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1
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109k
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Comment: C: What Are The Most Common Stupid Mistakes In Bioinformatics?
5.3 years ago by colindaven 8.0k
1
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0
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15k
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Comment: C: RNASeq user experience with Novogene?
5.4 years ago by colindaven 8.0k
1
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0
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664
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Answer: A: How to replace the chromosome seq from new chromosome sequence in genome file
5.4 years ago by colindaven 8.0k
1
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1
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4.3k
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Answer: A: Count total number of Homozygous/Heterozygous SNPs from VCF file
5.4 years ago by colindaven 8.0k
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1
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1.1k
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Answer: A: de novo transcriptome
5.4 years ago by colindaven 8.0k
1
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0
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1.4k
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Answer: A: Mapping using assembled contigs
5.4 years ago by colindaven 8.0k
0
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1
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869
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Answer: A: BLAST and GFF script to find locations of SNPs
5.4 years ago by colindaven 8.0k
0
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0
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1.9k
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Answer: A: RNA-seq Nanopore and Illumina hybrid assembly to improve gene annotation
5.4 years ago by colindaven 8.0k
0
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0
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2.0k
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Comment: C: Best practices to submit a multiple node job in cluster
5.4 years ago by colindaven 8.0k
5
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1
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1.3k
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Answer: A: What species are indicators of environmental contamination in metagenomic studie
5.4 years ago by colindaven 8.0k
1
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0
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5.8k
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Comment: C: Is it possible to directly convert fastq to CRAM ?
5.4 years ago by colindaven 8.0k
1
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1
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2.0k
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Answer: A: Private Database Schema for NGS results storage (Fastq, BAM, VCF...) ?
5.5 years ago by colindaven 8.0k
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0
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1.4k
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Answer: A: free linux server
5.5 years ago by colindaven 8.0k
2
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1
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1.0k
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Answer: A: Interpretation of sparse reads
5.5 years ago by colindaven 8.0k
1
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0
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6.8k
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Comment: C: BWA-MEM read groups usage
5.5 years ago by colindaven 8.0k
1
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1
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4.3k
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Comment: C: How to make GFF file based on assembled transcriptome and genome sequence?
5.5 years ago by colindaven 8.0k
1
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0
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2.3k
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Answer: A: Finding the cause for corrupt ChIP-Seq data
5.5 years ago by colindaven 8.0k
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0
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713
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Answer: A: Perform SNP-SNP correlation.
5.5 years ago by colindaven 8.0k
0
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0
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1.7k
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Comment: C: variant calling ecoli
5.5 years ago by colindaven 8.0k
1
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0
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2.2k
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Answer: A: Repeats detection in a genome
5.5 years ago by colindaven 8.0k
0
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0
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1.4k
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Answer: A: Using galaxy tool htseq_count for lncRNA in wheat reference genome
5.5 years ago by colindaven 8.0k
0
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0
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15k
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Answer: A: cellranger count help
5.5 years ago by colindaven 8.0k
1
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0
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876
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Answer: A: BWA, fastq reads mapped to multi ref fasta. ALL vs ALL
5.5 years ago by colindaven 8.0k
0
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0
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1.5k
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Comment: C: Polishing genome with pacbio reads
5.5 years ago by colindaven 8.0k
0
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1
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1.5k
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Comment: C: Polishing genome with pacbio reads
5.5 years ago by colindaven 8.0k
0
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0
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2.8k
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Answer: A: blasting a fasta file with many, many contigs via command line
5.6 years ago by colindaven 8.0k
10
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4
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13k
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Tutorial: Using the MinION MinKNOW software on Ubuntu 1604
long-reads oxford-nanopore minion
updated 2.5 years ago by 45k • written 6.2 years ago by 8.0k
0
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0
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3.1k
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Answer: A: Error when putting multiple read files in CITE-seq-Count
5.6 years ago by colindaven 8.0k
3
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0
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2.2k
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Answer: A: de novo annotation of plants genome
5.6 years ago by colindaven 8.0k
1
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0
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679
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Comment: C: Dealing with multiple-mapped reads in sRNA-seq
5.6 years ago by colindaven 8.0k
0
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0
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1.2k
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Comment: C: sparsehash FATAL ERROR: failed to allocate 19 groups
5.6 years ago by colindaven 8.0k
2
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1
reply
2.9k
views
Comment: C: Generate count table using Samtools
5.6 years ago by colindaven 8.0k
0
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0
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1.4k
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Answer: A: how to find haplotype of SNPs
5.6 years ago by colindaven 8.0k
0
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0
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1.0k
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Answer: A: Maker usage and tBLASTn
5.6 years ago by colindaven 8.0k
0
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0
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2.9k
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Comment: C: Generate count table using Samtools
5.6 years ago by colindaven 8.0k
1
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1
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4.7k
views
Comment: C: install bcl2fastq
5.6 years ago by colindaven 8.0k
0
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0
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989
views
Comment: C: Methods to convert SOLiD reads to nucleotide space
5.6 years ago by colindaven 8.0k
0
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1
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4.7k
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Comment: C: install bcl2fastq
5.6 years ago by colindaven 8.0k
0
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1
reply
989
views
Answer: A: Methods to convert SOLiD reads to nucleotide space
5.6 years ago by colindaven 8.0k
1
vote
1
reply
2.1k
views
Answer: A: Bam aligmnet file viewing.
5.6 years ago by colindaven 8.0k
1,105 results • Page 16 of 23
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