References
- 최무림, "차세대 시퀀싱 기법을 이용한 의학 유전체학의 발전 동향", 분자세포생물학뉴스레터, 2014년 4월.
- https://www.genome.gov/sequencingcostsdata/
- Schatz MC, Langmead B, Salzberg SL., "Cloud computing and the DNA data race," Nat Biotechno, 2010, Vol. 28, No. 7, pp. 691-693. https://doi.org/10.1038/nbt0710-691
- Baker M., "Next-generation sequencing: adjusting to data overload," Nat Meth, 2010, Vol. 7, No. 7, pp. 495-499. https://doi.org/10.1038/nmeth0710-495
- Calabrese B, Cannataro M., "Bioinformatics and microarray data analysis on the cloud," Meth Mol Biol, 2016, Vol. 1375, pp. 25-39.
- http://ngenebio.com/
- 이창용, "차세대 염기서열 데이터의 생물정보학적 분석", BRIC View 동향리포트,2016
- https://www.bioin.or.kr/board.do?cmd=view&bid=tech&num=216321
- BWA, https://github.com/lh3/bwa
- GATK, https://software.broadinstitute.org/gatk/
- Langmead B, Trapnell C, Pop M, Salzberg SL., "Ultrafast and memory-efficient alignment of short DNA sequences to the human genome," Genome biology, 2009 Mar 4, Vol. 10, No. 3.
- http://broadinstitute.github.io/picard/
- https://github.com/GregoryFaust/samblaster
- https://github.com/broadinstitute/mutect
- https://hpc.nih.gov/apps/MutSig.html
- https://github.com/ekg/freebayes
- https://github.com/WGLab/doc-ANNOVAR/
- https://www.ensembl.org/vep
- https://gencore.bio.nyu.edu/variant-calling-pipeline/
- https://wikis.utexas.edu/display/bioiteam/DNAseq+Variant+Calling+Pipeline
- https://hadoop.apache.org/
- https://spark.apache.org/
- Decap D, Reumers J, Herzeel C, Costanza P, Fostier J., "Halvade: scalable sequence analysis with MapReduce," Bioinformatics, 2015 Mar 26, Vol. 31, No. 15, pp. 2482-2488. https://doi.org/10.1093/bioinformatics/btv179
- https://github.com/citiususc/BigBWA
- https://github.com/citiususc/SparkBW
- Junehawk Lee, Hyeonbyeong Lee, Jihye Moon, Hyojin Kang, Seokil Song and Seok Jong Yu, "Paralleldistributed PCR duplication marking algorithm integrated with genome sequence alignment by using streaming technology," Proceedings of TBC 2017, 2017.