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Answer: Answer: treemix input issue
2.1 years ago by Gabriel R. ★ 2.9k
3
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1
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3.9k
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Answer: A: Demultiplexing based on dual indices in headers while allowing 1 mismatch to eac
3.9 years ago by Gabriel R. ★ 2.9k
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0
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1.4k
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Answer: A: Filter bam files based on length of contig
3.9 years ago by Gabriel R. ★ 2.9k
1
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1
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773
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Answer: A: Variation of the genotypes of the human MT chromosome
3.9 years ago by Gabriel R. ★ 2.9k
1
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1
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1.3k
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Answer: A: Calling chrMT only from BAM
4.0 years ago by Gabriel R. ★ 2.9k
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0
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8.3k
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Answer: A: Insert Size For Illumina Gaiix Paired-End Library From Sam/Bam File
4.4 years ago by Gabriel R. ★ 2.9k
1
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1
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1.8k
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Answer: A: How to use trimmed and merged outputs in bwa?
4.4 years ago by Gabriel R. ★ 2.9k
1
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0
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935
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Answer: A: Changing Whacky Fastq Quality for Demultiplexing
4.4 years ago by Gabriel R. ★ 2.9k
0
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1
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3.7k
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Answer: A: .pop file in ADMIXTURE
updated 4.4 years ago by 43k • written 8.5 years ago by ★ 2.9k
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0
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5.3k
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Answer: A: bcf convert 23andme to vcf
4.5 years ago by Gabriel R. ★ 2.9k
1
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1
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16k
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Answer: A: Sra Format Questions: How To Get A Sam File That Can Be Converted To Bam?
updated 4.5 years ago by 43k • written 10.2 years ago by ★ 2.9k
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0
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2.6k
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Answer: A: Need Help Interpreting The Genotype Fields In A Vcf Formatted Data
updated 4.6 years ago by 43k • written 10.9 years ago by ★ 2.9k
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0
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2.1k
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Answer: A: Allele count from BAM file
4.7 years ago by Gabriel R. ★ 2.9k
1
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0
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3.8k
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Answer: A: Convert vcf phased data to plink
4.8 years ago by Gabriel R. ★ 2.9k
0
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1
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1.5k
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Answer: A: deML: ERROR: Discrepancy between fastq files, different names with first index
5.0 years ago by Gabriel R. ★ 2.9k
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0
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5.3k
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Answer: A: Problem with demultiplexing illumina dual indexed libraries
5.1 years ago by Gabriel R. ★ 2.9k
0
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0
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24k
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Answer: A: Best trimming tool
5.1 years ago by Gabriel R. ★ 2.9k
1
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0
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1.6k
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Answer: A: Error when using deML with dual indexed paired end sequencs
5.1 years ago by Gabriel R. ★ 2.9k
2
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1
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3.5k
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Answer: A: Generating artificial NGS reads from a FASTA file specifying read length, covera
5.1 years ago by Gabriel R. ★ 2.9k
0
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0
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2.0k
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Answer: A: Low coverage genome simulation
5.3 years ago by Gabriel R. ★ 2.9k
0
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0
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30k
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Answer: Answer: Merge Paired-End Reads
updated 23 months ago by 43k • written 9.1 years ago by ★ 2.9k
2
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1
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2.9k
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Answer: A: What do you consider to be raw data from Illumina sequencers? Possible legacy d
5.4 years ago by Gabriel R. ★ 2.9k
0
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0
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3.4k
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Answer: A: Demultiplexing before merging paired-end reads?
5.4 years ago by Gabriel R. ★ 2.9k
1
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0
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889
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Answer: A: deML 'rgqual' parameter
5.6 years ago by Gabriel R. ★ 2.9k
5
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1
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2.9k
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Answer: A: Calculate average mapping quality at a position
5.7 years ago by Gabriel R. ★ 2.9k
3
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2
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11k
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Answer: A: Demultiplexing Illumina data
6.0 years ago by Gabriel R. ★ 2.9k
0
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0
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14k
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Answer: A: Getting data into Plink! and TreeMix
6.0 years ago by Gabriel R. ★ 2.9k
3
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0
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4.2k
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Answer: A: Help getting Plink files into Treemix
6.0 years ago by Gabriel R. ★ 2.9k
2
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1
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1.6k
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Answer: A: Variant with AD 14,3 is heterozygote?
6.0 years ago by Gabriel R. ★ 2.9k
4
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0
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1.3k
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Answer: A: How many reads needed to be sure a variant does not exist?
6.2 years ago by Gabriel R. ★ 2.9k
1
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1
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12k
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Answer: A: Can Illumina bcl2fastq use only one index for demultiplexing dual index sequenci
6.2 years ago by Gabriel R. ★ 2.9k
0
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0
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4.3k
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Answer: A: Split BAM file from more sample
6.4 years ago by Gabriel R. ★ 2.9k
0
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1
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2.7k
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Answer: A: Detection of deletion for mitochondrial NGS analysis at position 3107
6.4 years ago by Gabriel R. ★ 2.9k
2
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1
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1.6k
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Answer: A: Precedence between alt field and GT info in vcf files
6.4 years ago by Gabriel R. ★ 2.9k
2
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0
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2.0k
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Answer: A: Are there any tools to simulate mutations?
6.5 years ago by Gabriel R. ★ 2.9k
6
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0
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4.2k
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Answer: A: Do I need to merge bai files also, while merging bam files
6.5 years ago by Gabriel R. ★ 2.9k
0
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0
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2.5k
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Answer: A: simulating illumina data with spiked variants
6.7 years ago by Gabriel R. ★ 2.9k
2
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0
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6.5k
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Answer: A: weird insert size post trimming
6.7 years ago by Gabriel R. ★ 2.9k
6
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0
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7.9k
views
Answer: A: Programming Language In Bioinformatics
6.7 years ago by Gabriel R. ★ 2.9k
2
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0
replies
4.4k
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Answer: A: Why not merging?
6.8 years ago by Gabriel R. ★ 2.9k
1
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0
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4.9k
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Answer: A: Demultiplex dual index NextSeq run with only one barcode
6.9 years ago by Gabriel R. ★ 2.9k
0
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0
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2.4k
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Answer: A: BAM file statics and heterozygoty rate
6.9 years ago by Gabriel R. ★ 2.9k
1
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1
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2.9k
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Answer: A: Human Mitochondrial Variants Annotation
7.0 years ago by Gabriel R. ★ 2.9k
1
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0
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4.9k
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Answer: A: Theta Watterson on SNP
7.1 years ago by Gabriel R. ★ 2.9k
0
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2
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1.2k
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Answer: A: paired-end BAM file sequence search
7.2 years ago by Gabriel R. ★ 2.9k
1
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0
replies
4.4k
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Answer: A: Help: Read Sam File and find chromosome
7.2 years ago by Gabriel R. ★ 2.9k
1
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0
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5.0k
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Answer: A: shannon entropy score
7.4 years ago by Gabriel R. ★ 2.9k
0
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0
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2.0k
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Answer: A: How heterozygous GTs were defined in SNP calling vcf result
7.4 years ago by Gabriel R. ★ 2.9k
0
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0
replies
5.0k
views
Answer: A: bcl2fastq barcode collision detector error
7.6 years ago by Gabriel R. ★ 2.9k
5
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2
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3.7k
views
Answer: A: How to extract reads from BAM file and shuffle in another BAM to simulate a new
7.7 years ago by Gabriel R. ★ 2.9k
103 results • Page 1 of 3
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