PPT-Mapping NGS sequences to a reference genome
Author : debby-jeon | Published Date : 2016-05-27
Why Resequencing studies DNA Structural variation SNP identification RNAseq Mapping transcripts to a genome sequence Genome annotation Transcript enumeration Identification
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Mapping NGS sequences to a reference genome: Transcript
Why Resequencing studies DNA Structural variation SNP identification RNAseq Mapping transcripts to a genome sequence Genome annotation Transcript enumeration Identification of splice junctionsvariants. . Krumlov. January 2012. Mapping and variant calling. from short read data. Gerton Lunter. Wellcome. Trust Centre for Human Genetics. Oxford. June 26, 2000: “G-Day”. Completion of the Working Draft of the Human Genome. : Conifer Reference Genome Sequencing. An Adaptive Approach to the Sequencing of the Large Genomes of Multiple Conifer Species. Supported by USDA NIFA AFRI. U. California-Davis, CHORI, Johns Hopkins U.,. Bioinformatics. HW2. Papers. 1. . BLAT-. -The BLAST-Like Alignment Tool. 2. Classification . of DNA sequences using Bloom Filters. Course Intructor. Dr. Jianhua Ruan. Presenters. Husnu Narman. Nihat Altiparmak. Genome sequencing. Next Gen sequencing. Genomics = resources. genome maps. genome sequences. genome clones. DNA microarrays. whole gene collections. functional genomics!. 1980- 1998. 1977- 2003. DNA mapping. . Krumlov. January 2012. Mapping and variant calling. from short read data. Gerton Lunter. Wellcome. Trust Centre for Human Genetics. Oxford. June 26, 2000: “G-Day”. Completion of the Working Draft of the Human Genome. . Egusquiza. D145 Presentation. January 12, 2017. What is genome mapping?. http://www.yourgenome.org/facts/how-do-you-map-a-genome. The use of various methods to determine the locus of a genetic landmarks (genes, regulatory sites, etc.) and the relative distances between genetic landmarks in the genome. . Egusquiza. D145 Presentation. January 12, 2017. What is genome mapping?. http://www.yourgenome.org/facts/how-do-you-map-a-genome. The use of various methods to determine the locus of a genetic landmarks (genes, regulatory sites, etc.) and the relative distances between genetic landmarks in the genome. shinisaurus. . crocodilurus. Jian . gao. , . qiye. li, . zongji. . wang. , yang . zhou. , . paolo. . martelli. , fang li, . zijun. . xiong. , . jian. . wang. , . huanming. yang, and . guojie. . Derek M Bickhart . Animal Genomics and Improvement Laboratory . Research Geneticist (Animal) . derek.bickhart@ars.usda.gov . Phone: (301) 504-8679 Fax: (301) 504-8092. USDA disclaimer. Disclaimers: Mention of trade names, commercial products, or companies in this publication is solely for the purpose of providing specific information and does not imply recommendation or endorsement by the US Department of Agriculture over others not mentioned. . bioinformaticians. Class meetings: TR 3:30-4:50 MCGIL 2315. Office hours: M 3:00-5:00, W 4:00-5:00 CSE 4216. Contact: . mgymrek@ucsd.edu. Today’s schedule:. 3:30. -. 3:55. Sequence alignment. 4. :55-. Evolution occurs through a set of modifications to the DNA. These modifications include point mutations, insertions, deletions, and rearrangements. Seemingly diverse species (say mice and humans) share significant similarity (80-90%) in their genes. 15, 2021. dsenol@andrew.cmu.edu. . Committee: . Prof. Onur Mutlu (CMU, ETH Zurich). Prof. Saugata Ghose (CMU, UIUC). Prof. James C. Hoe (CMU). Prof. Can Alkan (Bilkent University). Figure 9.01. PCR Detection of . Sequence Tagged Site. Mapping large genomes requires many . genetic markers. . Those based solely on their unique sequences are known as sequence tagged sites (STS). These unique sequences may be amplified by PCR and mapped relative to each other. In practice, each STS is defined by a pair of specific PCR primers at its ends that generate a PCR fragment of defined length.. . https://damlasenolcali.github.io/. . Konstantinos Kanellopoulos, Joel . Lindegger. , Zulal . Bingol. , Gurpreet S. Kalsi, Ziyi Zuo, Can Firtina, Meryem Banu . Cavlak. , Jeremie S. Kim, Nika Mansouri Ghiasi, .
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