Nucleic acid sequencing data processing

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1. Chimera check1
2. Assembly
2.1. Assembly method2
2.2. Estimated error rate3
2.3. Method of calculation of error rate
3. Finishing strategy
3.1. Status4
3.2. Coverage5
3.3. Number of contigs6
4. Additional information
4.1. Relevant Standard Operating Procedures (SOPs)
4.2. Relevant electronic resources



Footnotes

1 State whether the data have been checked for chimeric sequence, and how.
2 How was the assembly done (e.g. with a text based assembler like phrap or a flowgram assembler).
3 The estimated error rate associated with the finished sequences (e.g., error rate of 1 in 1000 bp).
4 Was the genome project intended to produce a complete or draft genome.
5 The fold coverage of the sequencing expressed as 2x, 3x, 18x etc.
6 Number of contigs produced for the genome.



Sources

MIGS



Notes

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