SNP detection for massively parallel whole-genome resequencing

Medicin og biovidenskab

• Alleles 87%
• Consensus Sequence 68%
• Costs and Cost Analysis 18%
• Data Accuracy 31%
• Datasets 23%
• Diploidy 32%
• DNA 16%
• Genetic Variation 28%
• Genome 80%
• Haploidy 37%
• High-Throughput Nucleotide Sequencing 85%
• Scientific Experimental Error 46%
• Single Nucleotide Polymorphism 100%
• Technology 77%
• X Chromosome 67%