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Comment: C: paired-end BAM file sequence search
8.7 years ago by Gabriel R. ★ 2.9k
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1.7k
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Answer: A: paired-end BAM file sequence search
8.7 years ago by Gabriel R. ★ 2.9k
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1
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4.1k
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Comment: C: Filtering Overlapping Paired-end Reads
8.7 years ago by Gabriel R. ★ 2.9k
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4.1k
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Comment: C: Filtering Overlapping Paired-end Reads
8.7 years ago by Gabriel R. ★ 2.9k
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5.5k
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Answer: A: Help: Read Sam File and find chromosome
8.7 years ago by Gabriel R. ★ 2.9k
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1
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2.1k
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Comment: C: Detect sequencing errors with freebayes (or other software)
8.8 years ago by Gabriel R. ★ 2.9k
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6.4k
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Answer: A: shannon entropy score
8.9 years ago by Gabriel R. ★ 2.9k
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2.4k
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Answer: A: How heterozygous GTs were defined in SNP calling vcf result
9.0 years ago by Gabriel R. ★ 2.9k
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8.2k
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Comment: C: demultiplexing with fastq having barcode and primer sequence
9.0 years ago by Gabriel R. ★ 2.9k
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5.7k
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Comment: C: how to extract allele specific reads from bamfiles?
9.1 years ago by Gabriel R. ★ 2.9k
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5.6k
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Answer: A: bcl2fastq barcode collision detector error
9.1 years ago by Gabriel R. ★ 2.9k
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4.7k
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Comment: C: I am trying to load a BAM file (Whole Genome) to IGV but I can't see anything
9.1 years ago by Gabriel R. ★ 2.9k
2
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1
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4.6k
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Comment: C: How to extract reads from BAM file and shuffle in another BAM to simulate a new
9.2 years ago by Gabriel R. ★ 2.9k
5
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2
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4.6k
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Answer: A: How to extract reads from BAM file and shuffle in another BAM to simulate a new
9.2 years ago by Gabriel R. ★ 2.9k
0
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0
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4.6k
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Comment: C: How to extract reads from BAM file and shuffle in another BAM to simulate a new
9.2 years ago by Gabriel R. ★ 2.9k
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0
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26k
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Comment: C: single line fasta to mult line fasta
9.2 years ago by Gabriel R. ★ 2.9k
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0
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2.7k
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Comment: C: What parameters should be used for Seq-Gen?
9.3 years ago by Gabriel R. ★ 2.9k
1
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0
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3.9k
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Answer: A: Any tools available to generate fake raw reads from assembled genomes?
9.3 years ago by Gabriel R. ★ 2.9k
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0
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4.9k
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Comment: C: Demultiplex paired-end reads with dual primers and barcodes
9.3 years ago by Gabriel R. ★ 2.9k
2
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0
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2.2k
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Answer: A: best way to get chimp-human homologous sites
9.3 years ago by Gabriel R. ★ 2.9k
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0
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5.4k
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Comment: C: Looking for neanderthal genomes to download
9.4 years ago by Gabriel R. ★ 2.9k
6
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1
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5.4k
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Answer: A: Looking for neanderthal genomes to download
9.4 years ago by Gabriel R. ★ 2.9k
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1
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4.9k
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Comment: C: Demultiplex paired-end reads with dual primers and barcodes
9.4 years ago by Gabriel R. ★ 2.9k
1
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0
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10k
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Comment: C: Extracting last N bases of reads in FASTQ file
9.5 years ago by Gabriel R. ★ 2.9k
1
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0
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10k
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Comment: C: Extracting last N bases of reads in FASTQ file
9.5 years ago by Gabriel R. ★ 2.9k
0
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0
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2.5k
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Comment: C: Modifying barcode sequence in fq files
9.5 years ago by Gabriel R. ★ 2.9k
4
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1
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2.5k
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Answer: A: Modifying barcode sequence in fq files
9.5 years ago by Gabriel R. ★ 2.9k
1
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2
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2.0k
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Tool: DICE: Joint Estimation of Contamination, Error and Demography for Nuclear DNA from Ancient Humans
demography ancientDNA sequencing
updated 2.3 years ago by 45k • written 9.6 years ago by ★ 2.9k
0
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0
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2.0k
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Comment: C: DICE: Joint Estimation of Contamination, Error and Demography for Nuclear DNA fr
9.6 years ago by Gabriel R. ★ 2.9k
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0
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3.1k
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Comment: C: Calculation Of Theoretical Minimum Coverage Per Mutation Frequency
9.6 years ago by Gabriel R. ★ 2.9k
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0
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3.6k
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Comment: C: Extracting paired unmapped reads into fastq gives empty file
9.6 years ago by Gabriel R. ★ 2.9k
0
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1
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3.6k
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Comment: C: Extracting paired unmapped reads into fastq gives empty file
9.6 years ago by Gabriel R. ★ 2.9k
0
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0
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2.6k
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Comment: C: How to generate contact probability graph from mapped reads?
9.6 years ago by Gabriel R. ★ 2.9k
0
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0
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9.4k
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Comment: C: demultiplexing tool for dual-indexed paired-end illumina libraries
9.7 years ago by Gabriel R. ★ 2.9k
0
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1
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9.4k
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Comment: C: demultiplexing tool for dual-indexed paired-end illumina libraries
9.7 years ago by Gabriel R. ★ 2.9k
0
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1
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9.4k
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Comment: C: demultiplexing tool for dual-indexed paired-end illumina libraries
9.7 years ago by Gabriel R. ★ 2.9k
1
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1
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9.4k
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Answer: A: demultiplexing tool for dual-indexed paired-end illumina libraries
9.7 years ago by Gabriel R. ★ 2.9k
0
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0
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3.2k
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Comment: Comment: Haplotype matrix to genotype matrix
updated 3.3 years ago by 45k • written 9.7 years ago by ★ 2.9k
0
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1
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3.7k
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Comment: C: FASTQ / SAM file processing: combining base QUAL scores
9.8 years ago by Gabriel R. ★ 2.9k
0
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1
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4.1k
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Answer: A: How to deal with adapter dimers?
9.8 years ago by Gabriel R. ★ 2.9k
1
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0
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5.1k
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Comment: Comment: ADMIXTURE results - how can I determine what SNPs are associated with different
updated 3.0 years ago by 45k • written 10.2 years ago by ★ 2.9k
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1
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5.1k
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Answer: A: ADMIXTURE results - how can I determine what SNPs are associated with different
10.2 years ago by Gabriel R. ★ 2.9k
0
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0
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6.0k
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Comment: Comment: Cluster Locations In .Locs Vs .Fastq From Miseq
updated 3.0 years ago by 45k • written 10.2 years ago by ★ 2.9k
1
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0
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7.6k
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Answer: Answer: Pre-processing MiSeq Paired End data
updated 3.0 years ago by 45k • written 10.3 years ago by ★ 2.9k
1
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0
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11k
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Comment: C: Mirna-Seq Trimming And Mapping?
10.3 years ago by Gabriel R. ★ 2.9k
0
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1
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11k
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Comment: Comment: Mirna-Seq Trimming And Mapping?
updated 2.9 years ago by 45k • written 10.3 years ago by ★ 2.9k
0
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0
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4.0k
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Comment: Comment: gender SNP marker
updated 2.9 years ago by 45k • written 10.3 years ago by ★ 2.9k
5
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0
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4.0k
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Comment: Comment: gender SNP marker
updated 2.9 years ago by 45k • written 10.3 years ago by ★ 2.9k
4
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0
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2.5k
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Answer: A: Extracted the chrM portion of bam into a new bam with header
10.3 years ago by Gabriel R. ★ 2.9k
1
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1
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5.8k
views
Comment: Comment: Genomic Annotation of Intervals (yes, again)
updated 3.3 years ago by 45k • written 10.5 years ago by ★ 2.9k
406 results • Page 5 of 9
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