In this repository we report our code and analyses of publicly available genomic sequences of Human h-Cov19. All the data used here is provided by the laboratories that kindly shared information through GISAID.
This is an ongoing project. Please refer to todo if you would like to contribute on a certain topic.
Data Last update: July 18, 2020.
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Data update. We are processing data on Sherlock. Deposit the msa.fasta and metadata.tsv files from Gisaid into a folder named with the current date in /home/groups/juliapr/covid19/alignment/data/
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Data pre-processing. This code is available on Sherlock: /home/groups/juliapr/covid19/alignment/code/. Edit quality_check.R to change the name of the data folder. ml R Rscript quality_check.R > outqual20200718 This code will place two new files in your data folder.
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Subset_filter.R creates a fasta file per population (country and some states) ml R Rscript subset_filter.R >outfileter20200718
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Initial_distances.R Computes a vector the vector of hamming distances to the ancestral reference and the matrices of genetic distances
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sites_ref.R removes sites that are not in the reference sequence and subset_filter.R will filter sites that have more than 20% of missing data.
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Accessing the sequences is slow. You can subset data with subset.fasta function in subset_data.R.
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Indexing a large file and accessing it via the indexed file can be faster and more efficient. For an example, see subset_filter.R.
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Quick estimates are generated with fast_covid.R.
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Estimates of Mutation rate
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Population Structure
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Diversity (Effective population size) Preliminary
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Comparative Analyses
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Comparison to Surveillance Data
Julia Palacios (juliapr@stanford.edu)
Jaehee Kim
James Johndrow
Mackenzie Simper
Vladimir Minin
Leonardo Bonanno
Aaron Behr
Samyak Rajanala
Lorenzo Cappello
https://midasnetwork.us/covid-19/