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0
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4.6k
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Answer: A: unpaired R1 and R2 sequences
9.2 years ago by igor 13k
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13k
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Comment: C: What is the exact definition for scaffold?
9.2 years ago by igor 13k
1
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0
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5.6k
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Answer: A: how do I create vcf4.1 instead of 4.2
9.2 years ago by igor 13k
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2
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6.4k
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Comment: C: Assembling de novo with multiple versions of paired-end reads
9.2 years ago by igor 13k
0
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1
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6.4k
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Comment: C: Assembling de novo with multiple versions of paired-end reads
9.2 years ago by igor 13k
1
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13k
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Answer: A: rRNA detection (for contamination) in RNA-seq
9.2 years ago by igor 13k
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0
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2.3k
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Comment: C: Remove repetitive sequence of variable length from reads
9.2 years ago by igor 13k
1
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0
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2.3k
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Comment: C: Remove repetitive sequence of variable length from reads
9.2 years ago by igor 13k
3
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1
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2.3k
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Answer: A: Remove repetitive sequence of variable length from reads
9.2 years ago by igor 13k
0
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0
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6.4k
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Comment: C: Assembling de novo with multiple versions of paired-end reads
9.2 years ago by igor 13k
0
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1
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2.2k
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Answer: A: Total SNP calculation using command line vs picardtools
9.2 years ago by igor 13k
0
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1
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6.4k
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Comment: C: Assembling de novo with multiple versions of paired-end reads
9.2 years ago by igor 13k
1
vote
1
reply
6.4k
views
Answer: A: Assembling de novo with multiple versions of paired-end reads
9.2 years ago by igor 13k
0
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0
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6.4k
views
Comment: C: Assembling de novo with multiple versions of paired-end reads
9.2 years ago by igor 13k
0
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1
reply
6.4k
views
Comment: C: Assembling de novo with multiple versions of paired-end reads
9.2 years ago by igor 13k
0
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1
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43k
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Comment: C: ATAC-seq peak calling with MACS
9.2 years ago by igor 13k
1
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0
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10k
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Answer: A: How to Convert Illumina reports to Vcf files?
9.2 years ago by igor 13k
2
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1
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6.8k
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Comment: C: Can't open gz file
9.2 years ago by igor 13k
0
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1
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2.2k
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Answer: A: Are there any tools able to exclude specific bases (bias) from methylation calli
9.2 years ago by igor 13k
0
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0
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2.0k
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Answer: A: Annotated files that contain the sequence of genes and CDSs?
9.2 years ago by igor 13k
0
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0
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9.7k
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Comment: C: I am really pissed off by the bioinformatics software world. Do/can we have a be
9.2 years ago by igor 13k
1
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0
replies
9.7k
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Comment: C: I am really pissed off by the bioinformatics software world. Do/can we have a be
9.2 years ago by igor 13k
0
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0
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9.6k
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Comment: C: ENCODE ATAC-seq pipeline peak calling
9.2 years ago by igor 13k
0
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1
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9.6k
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Comment: C: ENCODE ATAC-seq pipeline peak calling
9.2 years ago by igor 13k
1
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0
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2.0k
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Answer: A: Any pipeline for variant calling for CLIA
9.2 years ago by igor 13k
1
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1
reply
5.8k
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Comment: C: Differential Open Chromatin Locations From Dnase-Seq Data
9.2 years ago by igor 13k
1
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3
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9.7k
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Comment: C: I am really pissed off by the bioinformatics software world. Do/can we have a be
9.2 years ago by igor 13k
0
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2
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9.7k
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Comment: C: I am really pissed off by the bioinformatics software world. Do/can we have a be
9.2 years ago by igor 13k
0
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1
reply
2.8k
views
Comment: C: Software to identify overrepresented k-mers in sequencing data
9.2 years ago by igor 13k
0
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1
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4.0k
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Comment: C: annotating a vcf file containing Structural Variants
9.2 years ago by igor 13k
2
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0
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16k
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Comment: C: How to tell which transcript is the canonical transcript?
9.2 years ago by igor 13k
2
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1
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4.0k
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Answer: A: annotating a vcf file containing Structural Variants
9.2 years ago by igor 13k
1
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0
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2.4k
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Answer: A: Find Mutations Frequencies by Cancer Type
9.2 years ago by igor 13k
2
votes
1
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26k
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Comment: C: merging two bigwig files
9.2 years ago by igor 13k
1
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0
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16k
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Comment: C: find positions of a short sequence in a genome
9.2 years ago by igor 13k
3
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0
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26k
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Answer: A: merging two bigwig files
9.2 years ago by igor 13k
0
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0
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16k
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Comment: C: find positions of a short sequence in a genome
9.2 years ago by igor 13k
1
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2
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16k
views
Comment: C: find positions of a short sequence in a genome
9.2 years ago by igor 13k
1
vote
1
reply
16k
views
Comment: C: find positions of a short sequence in a genome
9.2 years ago by igor 13k
1
vote
1
reply
16k
views
Comment: C: find positions of a short sequence in a genome
9.2 years ago by igor 13k
0
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0
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16k
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Comment: C: find positions of a short sequence in a genome
9.2 years ago by igor 13k
1
vote
3
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16k
views
Comment: C: find positions of a short sequence in a genome
9.2 years ago by igor 13k
0
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1
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16k
views
Comment: C: find positions of a short sequence in a genome
9.2 years ago by igor 13k
0
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1
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5.6k
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Comment: C: FastQC: box plots without boxes?
9.2 years ago by igor 13k
1
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0
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3.8k
views
Comment: C: Is there any NGS tool which produce long pairwise reads?
9.2 years ago by igor 13k
4
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1
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3.8k
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Answer: A: Is there any NGS tool which produce long pairwise reads?
9.2 years ago by igor 13k
0
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0
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5.4k
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Comment: C: fold enrichment calculation for exome sequencing
9.2 years ago by igor 13k
0
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0
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2.2k
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Answer: A: how to arrange data for pathway analysis ?
9.2 years ago by igor 13k
0
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2
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5.4k
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Comment: C: fold enrichment calculation for exome sequencing
9.2 years ago by igor 13k
1
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0
replies
5.4k
views
Comment: C: fold enrichment calculation for exome sequencing
9.2 years ago by igor 13k
1,531 results • Page 24 of 31
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