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Comparison of available tools for constructing libraries for next-generation sequencing
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Comparison of available tools for constructing libraries for next-generation sequencing
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Image Search Results


Comparison of available tools for constructing libraries for next-generation sequencing

Journal: Biology Methods & Protocols

Article Title: PrimerPooler: automated primer pooling to prepare library for targeted sequencing

doi: 10.1093/biomethods/bpx006

Figure Lengend Snippet: Comparison of available tools for constructing libraries for next-generation sequencing

Article Snippet: Based on the two DNA samples tested, both 50ng and 75ng starting amounts of DNA yielded very similar results, and similarly there was no obvious benefit when less diluted pre-amplified product (2.5 versus 5-fold dilution) was used for Fluidigm Access Array multiplex PCR ( ).

Techniques: Comparison, Multiplex Assay, Control

Coverage of targeted sequence regions by Fluidigm Access Array multiplex PCR and Illumina MiSeQ sequencing. Two FFPE DNA samples were tested under various experimental conditions including 50- and 75-ng DNA for pre-amplication, and 1l of 2.5- and 5.0-fold diluted pre-amplified products for Fluidigm Access Array multiplex PCR. An average of 3269 reads was achieved for the targeted regions, with 95% of targets covered by at least 50 reads, the minimal depth of reads for confident variant calling.

Journal: Biology Methods & Protocols

Article Title: PrimerPooler: automated primer pooling to prepare library for targeted sequencing

doi: 10.1093/biomethods/bpx006

Figure Lengend Snippet: Coverage of targeted sequence regions by Fluidigm Access Array multiplex PCR and Illumina MiSeQ sequencing. Two FFPE DNA samples were tested under various experimental conditions including 50- and 75-ng DNA for pre-amplication, and 1l of 2.5- and 5.0-fold diluted pre-amplified products for Fluidigm Access Array multiplex PCR. An average of 3269 reads was achieved for the targeted regions, with 95% of targets covered by at least 50 reads, the minimal depth of reads for confident variant calling.

Article Snippet: Based on the two DNA samples tested, both 50ng and 75ng starting amounts of DNA yielded very similar results, and similarly there was no obvious benefit when less diluted pre-amplified product (2.5 versus 5-fold dilution) was used for Fluidigm Access Array multiplex PCR ( ).

Techniques: Sequencing, Multiplex Assay, Amplification, Variant Assay