Method and device for quick contrast and analysis of short sequence for second-generation sequencing
A second-generation sequencing and analysis method technology, applied in the field of bioinformatics, can solve the problems of high memory usage and low efficiency of sequencing data comparison, and achieve the effects of fast comparison speed, shortened comparison time, and saving memory resources
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[0096] Example 1 Data analysis of non-invasive prenatal testing based on the rapid comparison and analysis method of short sequences of next-generation sequencing
[0097] The module flow of the present invention to realize the non-invasive prenatal detection first uses perl language and shell commands to preprocess the human reference genome hg19.fa, and process it into the format required by the index query library, including three columns:
[0098] The first column: 36-mer DNA sequence fragment;
[0099] The second column: the chromosome number where the fragment is located;
[0100] The third column: the position on the chromosome where the fragment is located.
[0101] Then its core method is realized based on C language algorithm and data structure.
[0102] The design process and operation of the present invention require hardware and software environment: Linux system; more than 3 cores; more than 35 memory; C library under the Linux platform; Gcc compiler; Gdb debug...
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