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- W1495079821 abstract "Protein isoforms make the transcriptome complex and challenging to resolve. Different forms of a protein may be produced from related genes or may arise from the same gene by alternative splicing. With a combination of long (400–500 bp) 454 Sequencing™ reads, dedicated GS De Novo Assembler software and a straightforward protocol using just 200 ng of RNA as sample input, the Genome Sequencer FLX System offers a powerful solution to help unravel the complexities of the transcriptome." @default.
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- W1495079821 date "2011-02-25" @default.
- W1495079821 modified "2023-09-23" @default.
- W1495079821 title "Comprehensive transcriptome analysis with the Genome Sequencer FLX System" @default.
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- W1495079821 doi "https://doi.org/10.1038/nmeth.f.338" @default.
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