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Designing CNV analysis assay on Digital PCR
dPCR mitochondrial DNA CNV
updated 3.8 years ago by • 0 • written 7.8 years ago by • 0
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0
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923
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Manipulation with coverage files/bedgraphs etc.
ngs sequencing sequence
updated 7.2 years ago by 89k • written 7.2 years ago by • 0
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0
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2.0k
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Comment: C: Importing data to excel spreadsheet - gene variant analysis
7.5 years ago by dominik.saburo • 0
2
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3
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2.0k
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Importing data to excel spreadsheet - gene variant analysis
sequencing gene SNP database
7.5 years ago by dominik.saburo • 0
12
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9
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2.5k
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7 follow
BRCA1 and BRCA2 database's for NGS diagnostics purposes
sequencing ngs database
updated 7.6 years ago by ★ 5.2k • written 7.6 years ago by • 0
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0
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2.5k
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Comment: A: BRCA1 and BRCA2 database's for NGS diagnostics purposes
7.6 years ago by dominik.saburo • 0
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0
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2.5k
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Comment: C: BRCA1 and BRCA2 database's for NGS diagnostics purposes
7.6 years ago by dominik.saburo • 0
0
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0
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2.5k
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Comment: C: BRCA1 and BRCA2 database's for NGS diagnostics purposes
7.6 years ago by dominik.saburo • 0
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0
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2.8k
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Comment: C: Displaying genes in genome browsers
7.8 years ago by dominik.saburo • 0
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1
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2.8k
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Comment: C: Displaying genes in genome browsers
7.9 years ago by dominik.saburo • 0
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6
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2.8k
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Displaying genes in genome browsers
sequencing next-gen
7.9 years ago by dominik.saburo • 0
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0
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2.8k
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Comment: A: Displaying genes in genome browsers
7.9 years ago by dominik.saburo • 0
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0
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1.6k
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Comment: C: NGS - Mapping quality of specific regions
8.2 years ago by dominik.saburo • 0
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3
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1.6k
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NGS - Mapping quality of specific regions
next-gen sequencing alignment
updated 8.2 years ago by ▴ 360 • written 8.2 years ago by • 0
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0
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1.0k
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Perfect gene investigation - ngs data clinical analysis step by step
snp next-gen sequencing
8.3 years ago by dominik.saburo • 0
0
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1
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3.8k
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Comment: C: FastQC report explanation on example
8.4 years ago by dominik.saburo • 0
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2
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3.8k
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Comment: C: FastQC report explanation on example
8.4 years ago by dominik.saburo • 0
2
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8
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3.8k
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FastQC report explanation on example
next-gen sequencing software error
updated 8.4 years ago by ★ 2.1k • written 8.4 years ago by • 0
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0
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2.4k
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Comment: C: Problems with proper interpretation of visualized bam file from Illumina Miniseq
8.4 years ago by dominik.saburo • 0
0
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1
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2.4k
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Comment: C: Problems with proper interpretation of visualized bam file from Illumina Miniseq
8.4 years ago by dominik.saburo • 0
0
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1
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2.4k
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Comment: C: Problems with proper interpretation of visualized bam file from Illumina Miniseq
8.4 years ago by dominik.saburo • 0
1
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7
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2.4k
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Problems with proper interpretation of visualized bam file from Illumina Miniseq platform
software error alignment sequencing next-gen SNP
8.4 years ago by dominik.saburo • 0
0
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1
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1.9k
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Answer: A: Software to identify and classify disease-relevant variants
8.5 years ago by dominik.saburo • 0
1
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3
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1.9k
views
Software to identify and classify disease-relevant variants
SNP next-gen
8.5 years ago by dominik.saburo • 0
24 results • Page 1 of 1
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