From Genome Analysis Wiki
Jump to navigationJump to search
248 bytes added
, 10:23, 2 February 2017
Line 1: |
Line 1: |
| + | '''Note:''' the latest version of this practical is available at: [[SeqShop: Estimates of Genetic Ancestry Practical]] |
| + | * The ones here is the original one from the June workshop (updated to be run from elsewhere) |
| + | |
| + | |
| == Introduction == | | == Introduction == |
| See the [[Media:LASER-tutorial.pdf|tutorial slides]] for an introduction of the LASER analysis workflow, input/output file formats, and usage of the LASER software. | | See the [[Media:LASER-tutorial.pdf|tutorial slides]] for an introduction of the LASER analysis workflow, input/output file formats, and usage of the LASER software. |
Line 4: |
Line 8: |
| The main purpose of this page is to provide step-by-step command lines for using LASER to estimate ancestry of 6 targeted sequenced samples (2 HapMap trios) in a principal component space generated using genome-wide SNP data from the Human Genome Diversity Project (HGDP). The HGDP reference panel contains genotype data across 632,958 autosomal loci for 938 individuals from 53 populations worldwide. | | The main purpose of this page is to provide step-by-step command lines for using LASER to estimate ancestry of 6 targeted sequenced samples (2 HapMap trios) in a principal component space generated using genome-wide SNP data from the Human Genome Diversity Project (HGDP). The HGDP reference panel contains genotype data across 632,958 autosomal loci for 938 individuals from 53 populations worldwide. |
| | | |
− | For more details about the options and usage of LASER, please read the [http://www.sph.umich.edu/csg/chaolong/LASER/LASER_Manual.pdf manual]. | + | For more details about the options and usage of LASER, please read the [http://csg.sph.umich.edu//chaolong/LASER/LASER_Manual.pdf manual]. |
| | | |
| == LASER workflow == | | == LASER workflow == |
Line 50: |
Line 54: |
| <div class="mw-collapsible-content"> | | <div class="mw-collapsible-content"> |
| | | |
− | This tutorial uses samtools from GotCloud, as well as example data downloaded in the Sequence Mapping & Assembly tutorial, so if you have not already installed GotCloud and the tutorial data in a previous tutorial, please do so now: [[SeqShop:_Sequence_Mapping_and_Assembly_Practical#Setup_when_running_on_your_own_outside_of_the_SeqShop_Workshop|Tutorial Setup]] | + | This tutorial uses samtools from GotCloud, as well as example data downloaded in the Sequence Mapping & Assembly tutorial, so if you have not already installed GotCloud and the tutorial data in a previous tutorial, please do so now: [[SeqShop:_Sequence_Mapping_and_Assembly_Practical, June 2014#Setup_when_running_on_your_own_outside_of_the_SeqShop_Workshop|Tutorial Setup]] |
| | | |
| | | |
Line 83: |
Line 87: |
| Download and decompress software package: | | Download and decompress software package: |
| | | |
− | wget http://www.sph.umich.edu/csg/chaolong/LASER/LASER-2.01.tar.gz | + | wget http://csg.sph.umich.edu//chaolong/LASER/LASER-2.01.tar.gz |
| tar xzvf LASER-2.01.tar.gz | | tar xzvf LASER-2.01.tar.gz |
− |
| |
| | | |
| == Preparing input files for LASER == | | == Preparing input files for LASER == |
Line 182: |
Line 185: |
| less -S hapmap_trios.SeqPC.coord | | less -S hapmap_trios.SeqPC.coord |
| | | |
− | The results should look like below: | + | The results should look like below (results will vary slightly): |
| | | |
| popID indivID L1 Ci K t PC1 PC2 PC3 PC4 | | popID indivID L1 Ci K t PC1 PC2 PC3 PC4 |