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Comment: C: How the strengths of Lisp-family languages facilitate building complex and flexi
8.7 years ago by Brian Bushnell 20k
2
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2.4k
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Comment: C: How the strengths of Lisp-family languages facilitate building complex and flexi
8.7 years ago by Brian Bushnell 20k
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4.2k
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Comment: C: Trying to Understand Global alignment Score
8.7 years ago by Brian Bushnell 20k
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4.2k
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Comment: C: Trying to Understand Global alignment Score
8.7 years ago by Brian Bushnell 20k
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3.4k
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Answer: A: Trinity - in silico normalization before/after trimmomatic?
8.7 years ago by Brian Bushnell 20k
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4.2k
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Comment: C: Trying to Understand Global alignment Score
8.7 years ago by Brian Bushnell 20k
1
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Answer: C: removing PCR duplicates from MedipSeq Data
8.7 years ago by Brian Bushnell 20k
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1.7k
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Comment: C: VelvetK long Kmers
8.7 years ago by Brian Bushnell 20k
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3.3k
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Comment: C: Metagenomic data assembly.
8.7 years ago by Brian Bushnell 20k
7
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4.1k
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Answer: A: Phased - Unphased genotypes
8.7 years ago by Brian Bushnell 20k
1
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1
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4.3k
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Answer: A: tophat aligns to wrong strand
8.7 years ago by Brian Bushnell 20k
1
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2.6k
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Comment: C: Question about k-mer genie output
8.7 years ago by Brian Bushnell 20k
1
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6.2k
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Comment: C: RPKM and FPKM directly comparable?
8.7 years ago by Brian Bushnell 20k
7
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6.2k
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Answer: C: RPKM and FPKM directly comparable?
8.7 years ago by Brian Bushnell 20k
1
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1.8k
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Answer: A: Where I find plant example (small) dataset from Illumina Hiseq 2000 sequencing
8.8 years ago by Brian Bushnell 20k
0
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2.1k
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Answer: A: Understanding the key concept of per gene coverage in context to WGS
8.8 years ago by Brian Bushnell 20k
4
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13k
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Comment: C: Is going back to the wet lab worth it?
8.8 years ago by Brian Bushnell 20k
0
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1
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3.3k
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Answer: A: Metagenomic data assembly.
8.8 years ago by Brian Bushnell 20k
0
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1
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3.1k
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Comment: C: Trouble with installation Trinity on Linux 32 bit
8.8 years ago by Brian Bushnell 20k
0
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1.4k
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Comment: C: requirements for denovo rnaseq analysis
8.8 years ago by Brian Bushnell 20k
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1
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4.1k
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Comment: C: Check Kmer Count Results
8.8 years ago by Brian Bushnell 20k
1
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3.7k
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Comment: C: Demultiplex fastq files in which barcodes and primers are already removed
8.8 years ago by Brian Bushnell 20k
2
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1
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3.7k
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Comment: C: Demultiplex fastq files in which barcodes and primers are already removed
8.8 years ago by Brian Bushnell 20k
1
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2.0k
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Comment: C: Samtools mpileup - Individual Pile-ups vs Group Pile-ups
8.8 years ago by Brian Bushnell 20k
0
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1
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4.9k
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Answer: A: Demultiplex paired-end reads with dual primers and barcodes
8.8 years ago by Brian Bushnell 20k
1
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1
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12k
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Comment: C: BAM to FASTQ
8.8 years ago by Brian Bushnell 20k
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2.8k
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Comment: C: The future of third-generation sequencing
8.8 years ago by Brian Bushnell 20k
3
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1
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2.8k
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Comment: C: The future of third-generation sequencing
8.8 years ago by Brian Bushnell 20k
1
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1
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2.8k
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Answer: A: The future of third-generation sequencing
8.8 years ago by Brian Bushnell 20k
0
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0
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2.6k
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Comment: C: Variant calling - display nucleotides with 0 coverage
8.8 years ago by Brian Bushnell 20k
1
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1
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2.0k
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Comment: C: Samtools mpileup - Individual Pile-ups vs Group Pile-ups
8.8 years ago by Brian Bushnell 20k
0
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1
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2.6k
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Comment: C: Variant calling - display nucleotides with 0 coverage
8.8 years ago by Brian Bushnell 20k
0
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1
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2.4k
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Comment: C: Dating Common Ancestor
8.8 years ago by Brian Bushnell 20k
0
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1
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2.6k
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Comment: C: Variant calling - display nucleotides with 0 coverage
8.8 years ago by Brian Bushnell 20k
0
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1
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2.0k
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Comment: C: How to output all variant alleles at a given site, regardless of quality
8.8 years ago by Brian Bushnell 20k
0
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3.0k
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Comment: C: Variant Calling - for multiple samples need advice
8.8 years ago by Brian Bushnell 20k
1
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0
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12k
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Comment: C: BAM to FASTQ
8.8 years ago by Brian Bushnell 20k
1
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0
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12k
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Comment: C: BAM to FASTQ
8.8 years ago by Brian Bushnell 20k
0
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2
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3.0k
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Answer: A: Variant Calling - for multiple samples need advice
8.8 years ago by Brian Bushnell 20k
2
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3
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12k
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Answer: A: BAM to FASTQ
8.8 years ago by Brian Bushnell 20k
0
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1
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5.3k
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Comment: C: Calculate percentage mapped reads from Bowtie2/RSEM
8.8 years ago by Brian Bushnell 20k
2
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1
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2.0k
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Answer: A: How to output all variant alleles at a given site, regardless of quality
8.8 years ago by Brian Bushnell 20k
0
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0
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5.0k
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Comment: C: Data repository for Whole Exome Sequencing
8.8 years ago by Brian Bushnell 20k
0
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1
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2.5k
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Comment: C: Pseudogenes-Can we use them?
8.8 years ago by Brian Bushnell 20k
0
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1
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2.5k
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Comment: C: Pseudogenes-Can we use them?
8.8 years ago by Brian Bushnell 20k
0
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1
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2.5k
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Answer: A: Pseudogenes-Can we use them?
8.8 years ago by Brian Bushnell 20k
0
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1
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4.8k
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Comment: C: How to get percentage of reads mapped to each Reference Genome
8.8 years ago by Brian Bushnell 20k
0
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1
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3.0k
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Comment: C: sra to fastq conversion - paired-end file won't split
8.8 years ago by Brian Bushnell 20k
1
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0
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8.8k
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Comment: C: What is default paprameter of BWA mem mapping
8.8 years ago by Brian Bushnell 20k
1
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0
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7.0k
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Comment: C: bwa mem: which parameters to tune to improve alignment?
8.8 years ago by Brian Bushnell 20k
2,083 results • Page 25 of 42
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