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Questions and Answers
What methods are used in genomic analysis?
What is a characteristic of Next Generation Sequencing (NGS)?
What are some techniques used in Next Generation Sequencing (NGS)?
What is an amplification approach used in NGS?
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What is the time per Paired End (PED) run for ABI SOLiD sequencing?
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Which sequencing method is subject to error if a single region is not read multiple times?
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What is the characteristic of high-throughput sequencing (NGS) mentioned in the text?
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Which approach is used for amplification in Illumina/Solexa sequencing?
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What is the approximate number of samples per batch in Sanger sequencing?
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Which method is based on massive parallel sequencing?
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What is the primary role of bioinformatics in genomic analysis?
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What is the main challenge associated with high-throughput sequencing (NGS)?
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What is a distinguishing feature of next generation sequencing (NGS) compared to Sanger sequencing?
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Which method is used in next generation sequencing (NGS) to line up the reads and is subject to error if a single region is not read multiple times?
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Which sequencing technique is known for its use of polymerase-based sequence-by-synthesis?
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What is the typical size of paired end (PED) separation in next generation sequencing (NGS)?
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Which approach is used in next generation sequencing (NGS) to amplify DNA fragments in a massively parallel manner?
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What is a key advantage of next generation sequencing (NGS) over traditional Sanger sequencing?
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