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Answer:
Answer: Sanger Imputation Server - genotype probability distribution
2.6 years ago by
Dan
▴ 540
2
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0
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5.6k
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Answer:
A: Convert an 'intron-style' GFF3 file into an 'exon-style' GFF3 file
updated 4.8 years ago by
Ram
44k • written 10.4 years ago by
Dan
▴ 540
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7.5k
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Answer:
A: Phylogenetic tree of species
updated 4.8 years ago by
Ram
44k • written 10.4 years ago by
Dan
▴ 540
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2.8k
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Answer:
A: Difference between RepeatMasker and RepeatMasker viz.
updated 4.9 years ago by
Ram
44k • written 8.9 years ago by
Dan
▴ 540
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18k
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Answer:
A: How To Determine The Version Used To Generate Solexa/Illumina Fastq Files?
updated 6.1 years ago by
Ram
44k • written 12.1 years ago by
Dan
▴ 540
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Answer:
A: How To Determine The Version Used To Generate Solexa/Illumina Fastq Files?
updated 6.1 years ago by
Ram
44k • written 12.1 years ago by
Dan
▴ 540
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0
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4.2k
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Answer:
A: How to dump genes from GenBank in GFF3 format?
7.3 years ago by
Dan
▴ 540
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2.3k
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Answer:
A: Where To Find Probe Sequences For Agilent Microarray?
7.5 years ago by
Dan
▴ 540
2
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13k
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Answer:
A: Generate Consensus sequence from BAM file
7.6 years ago by
Dan
▴ 540
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3.5k
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Answer:
Answer: How does plink guess the reference base in "--recode vcf-iid"
updated 23 months ago by
Ram
44k • written 9.3 years ago by
Dan
▴ 540
0
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10k
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Answer:
Answer: PLINK: Convert bed,bim, fam to vcf file
updated 23 months ago by
Ram
44k • written 9.3 years ago by
Dan
▴ 540
5
votes
2
replies
5.6k
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Answer:
Answer: Convert an 'intron-style' GFF3 file into an 'exon-style' GFF3 file
updated 3.0 years ago by
Ram
44k • written 10.4 years ago by
Dan
▴ 540
1
vote
1
reply
2.2k
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Answer:
A: Retrieve GO terms for all completed genomes in GenBank
10.4 years ago by
Dan
▴ 540
1
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1
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7.4k
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Answer:
C: Plotting chromosomal data from sliding window analyses
10.4 years ago by
Dan
▴ 540
3
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0
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18k
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Answer:
Answer: Vcf Validator From Vcf Tools
updated 3.1 years ago by
Ram
44k • written 10.5 years ago by
Dan
▴ 540
0
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0
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4.2k
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Answer:
A: Is There A Package To Map Primer Pair On Genome In R/Bioconductor?
11.2 years ago by
Dan
▴ 540
2
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0
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3.5k
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Answer:
A: Structural Variants Standard Dataset
11.6 years ago by
Dan
▴ 540
1
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2
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4.5k
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Answer:
A: Genotype Likelihood In 1000 Genomes Vcf Data
11.6 years ago by
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▴ 540
4
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1
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2.9k
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Answer:
A: Which Sequences Should I Include In A Whole Genome Alignment Of Primates?
11.6 years ago by
Dan
▴ 540
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0
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4.1k
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Answer:
A: Exact Matching With Bowtie, Blat And Blast+
11.6 years ago by
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▴ 540
2
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0
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6.2k
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Answer:
A: How To Transform The Colorspace Data Obtained From Sra Into A Format Suitable Fo
11.7 years ago by
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▴ 540
4
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3
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3.4k
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Answer:
A: Publish Our Own Project
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▴ 540
0
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0
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1.8k
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Answer:
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11.7 years ago by
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▴ 540
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1
reply
4.1k
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Answer:
A: Translate A Nucleotide Alignment To Protein Alignment
11.7 years ago by
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▴ 540
1
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1
reply
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Answer:
A: Plotting Exon Statistics In R
11.7 years ago by
Dan
▴ 540
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