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1
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Comment: C: local alignment with a sets of sequences in a fasta file to a reference sequence
9.1 years ago by lh3 33k
0
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1
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3.8k
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Comment: C: How I can increase the length of contig in denovo assembly
9.2 years ago by lh3 33k
1
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4.2k
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Comment: C: Generating consensus sequences without reference genome
9.2 years ago by lh3 33k
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3.8k
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Answer: A: How I can increase the length of contig in denovo assembly
9.2 years ago by lh3 33k
1
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2
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3.8k
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Comment: C: How I can increase the length of contig in denovo assembly
9.2 years ago by lh3 33k
0
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1
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7.3k
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Comment: C: Minimum length of reads after trimming for Assembly
9.2 years ago by lh3 33k
1
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1
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7.3k
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Comment: C: Minimum length of reads after trimming for Assembly
9.2 years ago by lh3 33k
1
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0
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3.4k
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Comment: C: FREEBAYE vcf file and Snpsift error
9.2 years ago by lh3 33k
0
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1
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7.3k
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Comment: C: Minimum length of reads after trimming for Assembly
9.2 years ago by lh3 33k
5
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1
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6.7k
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Answer: A: diferent contigs chrM
9.2 years ago by lh3 33k
0
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17k
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Comment: C: Qual score in VCF file
9.3 years ago by lh3 33k
1
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3.5k
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Comment: C: Samtools view: Sequence of reads given by samtools view differs from read sequen
9.3 years ago by lh3 33k
0
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1
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2.9k
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Comment: C: Does the mapper can map the illumina reads exactly to the super-scaffolds
9.3 years ago by lh3 33k
3
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0
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3.1k
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Comment: C: SNP calling for correcting errors ?
9.3 years ago by lh3 33k
6
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4
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18k
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Answer: C: Retrieve a subset of FASTA from large multi-FASTA file
9.3 years ago by lh3 33k
2
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1
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3.5k
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Answer: A: insert size discrepencies using bwa backtrack and bwa mem
9.3 years ago by lh3 33k
0
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1
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4.1k
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Comment: C: Non-cancer somatic mutation calling
9.3 years ago by lh3 33k
1
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1
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4.3k
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Answer: A: Where to download raw HGDP data used for population genetics studies
9.4 years ago by lh3 33k
2
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0
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3.5k
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Answer: A: Adding a new gene to a precomputed gene tree ?
9.4 years ago by lh3 33k
1
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1
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3.6k
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Comment: C: Very slow Bio-linux on VirtualBox?
9.4 years ago by lh3 33k
0
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1
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2.8k
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Answer: A: Genome assembly process
9.4 years ago by lh3 33k
4
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4.0k
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Comment: C: Customize fasta headers
9.4 years ago by lh3 33k
2
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0
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7.5k
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Comment: C: How do I remove polymorphisms that failed filtering from a vcf file?
9.4 years ago by lh3 33k
0
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1
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2.7k
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Comment: C: Help with Bowtie2
9.4 years ago by lh3 33k
2
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0
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8.2k
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Comment: C: How to treat the unpaired data after trimmomatic
9.4 years ago by lh3 33k
0
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1
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2.1k
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Answer: A: Coverage/Read Depth per SNP in 1000Genomes
9.4 years ago by lh3 33k
0
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1
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2.4k
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Comment: C: Allelic Depth 1000 Genomes call set
9.4 years ago by lh3 33k
2
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0
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2.3k
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Comment: C: Does Treemix support multithreaded analyses?
9.4 years ago by lh3 33k
1
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1
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3.2k
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Comment: C: How to install clustalw in linux format for windows 10??
9.4 years ago by lh3 33k
0
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0
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5.0k
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Comment: C: Splitting fastq from stdin into multiple files ?
9.4 years ago by lh3 33k
0
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0
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4.1k
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Comment: C: Reason for Freebayes Calling Multi-base Variants
9.4 years ago by lh3 33k
4
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1
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4.7k
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Comment: C: Java or C++ (which side should I choose)
9.4 years ago by lh3 33k
0
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0
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3.5k
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Comment: C: detection of in/del in sanger sequencing
9.4 years ago by lh3 33k
1
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0
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4.7k
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Comment: C: Java or C++ (which side should I choose)
9.4 years ago by lh3 33k
5
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0
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3.1k
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Comment: C: 10 to 1000X speedup of BWA read alignment trough compressive mapping: MIT CORA
9.4 years ago by lh3 33k
0
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1
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3.5k
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Comment: C: detection of in/del in sanger sequencing
9.4 years ago by lh3 33k
5
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1
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3.5k
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Comment: C: What does "integrative call set" mean to you?
9.4 years ago by lh3 33k
2
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2
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3.1k
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Comment: C: 10 to 1000X speedup of BWA read alignment trough compressive mapping: MIT CORA
9.4 years ago by lh3 33k
1
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1
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22k
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Comment: C: pybam - 100% python BAM reader
9.4 years ago by lh3 33k
0
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0
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1.7k
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Comment: C: Trios from 1kG
9.4 years ago by lh3 33k
1
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1
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2.4k
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Comment: C: What if I break my VCF file into small VCF files and then generate Haplotype ind
9.4 years ago by lh3 33k
1
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1
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3.6k
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Comment: C: How do tools parse the QNAME?
9.4 years ago by lh3 33k
2
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0
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4.6k
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Comment: C: What are the most popular NGS tools?
9.4 years ago by lh3 33k
0
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0
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5.1k
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Comment: C: Unzipping bz2 files
9.4 years ago by lh3 33k
0
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0
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22k
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Comment: C: pybam - 100% python BAM reader
9.5 years ago by lh3 33k
0
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0
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6.8k
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Comment: C: Blast raw score calculation
9.5 years ago by lh3 33k
2
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0
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22k
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Comment: C: pybam - 100% python BAM reader
9.5 years ago by lh3 33k
2
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1
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2.5k
views
Comment: C: How to find number of unique n-mers in genome?
9.5 years ago by lh3 33k
138
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27
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53k
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14 follow
Why Are There Many Rna-Seq Hits To Intronic Regions?
rna-seq
updated 3.4 years ago by 45k • written 13.4 years ago by 33k
3
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1
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9.4k
views
Comment: C: Finding a specific gene in a fastq file without mapping the reads?
9.5 years ago by lh3 33k
1,458 results • Page 4 of 30
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