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Comment: C: Extracting randomly subset of fastq reads from a huge file
7.4 years ago by Brian Bushnell 20k
1
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13k
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Answer: A: Extracting randomly subset of fastq reads from a huge file
7.4 years ago by Brian Bushnell 20k
0
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1
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2.8k
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Comment: C: Is it possible to get VCF from two fastq files without reference genome?
7.4 years ago by Brian Bushnell 20k
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1.8k
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Comment: C: Bowtie2 output alignments and non-alignments in same file
7.4 years ago by Brian Bushnell 20k
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1.8k
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Answer: C: Bowtie2 output alignments and non-alignments in same file
7.4 years ago by Brian Bushnell 20k
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4.8k
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Comment: C: Keep one SNP for duplicate SNPs
7.4 years ago by Brian Bushnell 20k
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2
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4.6k
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Comment: C: error correction using BBTools
7.4 years ago by Brian Bushnell 20k
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1
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4.8k
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Comment: C: Keep one SNP for duplicate SNPs
7.4 years ago by Brian Bushnell 20k
1
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1
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5.2k
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Comment: C: Trim Illumina PE data with trimmomatic
7.4 years ago by Brian Bushnell 20k
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1
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4.8k
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Comment: C: Keep one SNP for duplicate SNPs
7.4 years ago by Brian Bushnell 20k
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1.2k
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Answer: A: what is the lowest coverage the human genome can be sequenced at to provide roug
7.4 years ago by Brian Bushnell 20k
1
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5.5k
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Comment: C: Indexing a genome
7.4 years ago by Brian Bushnell 20k
3
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1
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4.6k
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Answer: A: error correction using BBTools
7.4 years ago by Brian Bushnell 20k
0
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0
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6.6k
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Comment: C: HiSeq 4000 PhiX screening and removal using bbduk
7.4 years ago by Brian Bushnell 20k
1
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0
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5.0k
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Comment: C: Tips for increasing metaSPAdes assembly speed for 7 billion reads?
7.4 years ago by Brian Bushnell 20k
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0
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2.2k
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Comment: C: Number of sequence copies per cluster on Illumina?
7.4 years ago by Brian Bushnell 20k
0
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1
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2.2k
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Comment: C: Number of sequence copies per cluster on Illumina?
7.4 years ago by Brian Bushnell 20k
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0
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7.5k
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Comment: C: weird insert size post trimming
7.4 years ago by Brian Bushnell 20k
1
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1
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6.6k
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Comment: C: HiSeq 4000 PhiX screening and removal using bbduk
7.4 years ago by Brian Bushnell 20k
0
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0
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7.5k
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Comment: C: weird insert size post trimming
7.4 years ago by Brian Bushnell 20k
2
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2
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6.6k
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Comment: C: HiSeq 4000 PhiX screening and removal using bbduk
7.4 years ago by Brian Bushnell 20k
2
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1
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6.6k
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Comment: C: HiSeq 4000 PhiX screening and removal using bbduk
7.4 years ago by Brian Bushnell 20k
0
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2
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3.8k
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Comment: C: RNA-Seq or Exome Seq for Clinical data analysis
7.4 years ago by Brian Bushnell 20k
3
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1
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3.8k
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Answer: A: RNA-Seq or Exome Seq for Clinical data analysis
7.4 years ago by Brian Bushnell 20k
3
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0
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6.6k
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Comment: C: HiSeq 4000 PhiX screening and removal using bbduk
7.4 years ago by Brian Bushnell 20k
2
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1
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2.7k
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Comment: C: sequence in different line
7.4 years ago by Brian Bushnell 20k
1
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6.8k
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Answer: A: How to extract contigs from FASTA file which contains specific sequence
7.4 years ago by Brian Bushnell 20k
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7.0k
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Comment: C: understanding contig statistics
7.4 years ago by Brian Bushnell 20k
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0
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37k
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Comment: C: Duplicates on Illumina
7.4 years ago by Brian Bushnell 20k
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0
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37k
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Comment: C: Duplicates on Illumina
7.4 years ago by Brian Bushnell 20k
0
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0
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3.9k
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Comment: C: Splitting a fasta file on the basis of header barcodes
7.4 years ago by Brian Bushnell 20k
0
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1
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3.4k
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Comment: C: how to find strand information for a list of SNPs?
7.4 years ago by Brian Bushnell 20k
1
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0
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2.2k
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Comment: C: Base recalibration for data cleanup
7.4 years ago by Brian Bushnell 20k
0
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1
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2.2k
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Comment: C: Base recalibration for data cleanup
7.4 years ago by Brian Bushnell 20k
0
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0
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18k
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Comment: C: Reliable Fastq compression programs
7.4 years ago by Brian Bushnell 20k
0
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0
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16k
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Comment: C: Lossless ALAPY Fastq Compressor (now for MacOS X with 10-20% improved speed and
7.4 years ago by Brian Bushnell 20k
1
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1
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2.5k
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Comment: C: Where i can find sequencing reads(3rd generation sequencing) data set in which e
7.4 years ago by Brian Bushnell 20k
0
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1
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3.0k
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Comment: C: Add taxID for each record of a fasta file
7.4 years ago by Brian Bushnell 20k
2
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2
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3.0k
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Answer: A: Add taxID for each record of a fasta file
7.4 years ago by Brian Bushnell 20k
0
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0
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3.0k
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Comment: C: multiple Fastq file alignment
7.4 years ago by Brian Bushnell 20k
0
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0
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2.5k
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Answer: A: Finding of origin of replication in a bacterial Genome
7.4 years ago by Brian Bushnell 20k
0
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0
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5.9k
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Comment: C: Minimum length of reads
7.4 years ago by Brian Bushnell 20k
2
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0
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4.1k
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Answer: A: How to split forward and reverse reads from one fastq file?
7.4 years ago by Brian Bushnell 20k
0
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1
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5.9k
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Comment: C: Minimum length of reads
7.4 years ago by Brian Bushnell 20k
1
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2
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2.5k
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Comment: C: Where i can find sequencing reads(3rd generation sequencing) data set in which e
7.4 years ago by Brian Bushnell 20k
1
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0
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2.1k
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Comment: C: de novo SNP development from pool seq
7.4 years ago by Brian Bushnell 20k
1
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0
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3.9k
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Comment: C: counting ERCCs spike-ins in RNAseq data
7.4 years ago by Brian Bushnell 20k
2
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0
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2.4k
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Answer: A: Variant calling step order question: base recalibration & mark duplicates, which
7.4 years ago by Brian Bushnell 20k
0
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0
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3.8k
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Comment: C: How can I create a dummy dataset from my NGS whole-exome data?
7.4 years ago by Brian Bushnell 20k
2
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0
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2.6k
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Comment: C: [Solved] Differentiating between chromosomal and plasmid DNA
7.4 years ago by Brian Bushnell 20k
2,080 results • Page 11 of 42
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