Last updated: 2021-01-21

Checks: 7 0

Knit directory: TARI_2020GS/

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Unstaged changes:
    Modified:   output/TARI_trials_NOT_identifiable.csv
    Modified:   output/maxNOHAV_byStudy.csv

Note that any generated files, e.g. HTML, png, CSS, etc., are not included in this status report because it is ok for generated content to have uncommitted changes.


These are the previous versions of the repository in which changes were made to the R Markdown (analysis/index.Rmd) and HTML (docs/index.html) files. If you’ve configured a remote Git repository (see ?wflow_git_remote), click on the hyperlinks in the table below to view the files as they were in that past version.

File Version Author Date Message
Rmd ac1cf61 wolfemd 2021-01-21 Kibaha samples added. Cross-validation and predictions redone.
html abaf52a wolfemd 2020-12-23 Build site.
Rmd 9c8d010 wolfemd 2020-12-23 Start workflowr project.
Rmd 3d46094 wolfemd 2020-12-15 Start workflowr project.

This repository and website documents all analyses, summary, tables and figures associated with TARI genomic prediction and related procedures (e.g. imputation).

December Imputations

DCas20_5629

GS C1.

Impute with E. Africa Imputation Reference Panel dataset, which can be found on the Cassavabase FTP server here with names e.g. chr*_ImputationReferencePanel_StageVI_91119.vcf.gz with code/documentation here.

Steps:

  1. Convert DCas20_5629 report to VCF for imputation:
  2. Impute DCas20_5629: with East Africa reference panel

Files:

  • RefPanel VCF filename: chr*_ImputationReferencePanel_StageVI_91119.vcf.gz
  • Imputed filename: chr*_DCas20_5629_EA_REFimputed.vcf.gz
  • Post-impute filtered filename: chr*_DCas20_5629_EA_REFimputedAndFiltered.vcf.gz
  • Genome-wide dosage matrix format for use in R:
    • Imputation Reference Panel: DosageMatrix_ImputationReferencePanel_StageVI_91119.rds
    • DCas20_5629 with standard post-impute filter: DosageMatrix_DCas20_5629_EA_REFimputedAndFiltered.rds

HOW TO COMBINE DOSAGE MATRICES: Users will want to combine the genotypes in the imputation reference panel files, with the genotypes in the imputed DArT file. They can have slightly different sets of markers along the columns. Here is a basic example how to combine:

snps_refpanel<-readRDS("DosageMatrix_ImputationReferencePanel_StageVI_91119.rds")
snps_dcas20_5629<-readRDS("DosageMatrix_DCas20_5629_EA_REFimputedAndFiltered.rds")

snps2keep<-colnames(snps_refpanel)[,colnames(snps_refpanel) %in% colnames(snps_dcas20_5629)]
snps<-bind_rows(snps_refpanel[,snps2keep],
                snps_dcas20_5629[,snps2keep])

Genomic Prediction (Dec. 20 - Jan. 21)

Get TARI TP data from Cassavabase. Use it with imputed data to predict GEBV/GETGV for all samples in the new reports (DCas20-5629).

  1. Prepare training dataset: Download data from DB, “Clean” and format DB data.
    • [UPDATED Jan. 21, 2021]: Matches of germplasmName-to-FullSampleName (GBS and DArTseqLD records) improved for TARI.
    • All subsequent analyses re-run.
  2. Get BLUPs combining all trial data: Combine data from all trait-trials to get BLUPs for downstream genomic prediction.
    • Fit mixed-model to multi-trial dataset and extract BLUPs, de-regressed BLUPs and weights. Include two rounds of outlier removal.
  3. Check prediction accuracy: Evaluate prediction accuracy with cross-validation.
  4. Genomic prediction: Predict genomic BLUPs (GEBV and GETGV) for all selection candidates using all available data.
  5. Results: Plots, results and recommendations.
      1. Accuracy estimates are most improved relative to previously. I didn’t run the precise cross-validation folds so the judgement is based on visual comparison to the Dec. 2020 plot.
      1. DYLD and FYLD are not well predicted and I would not recommend using them based on selection.
      1. Expected Genetic Gain: GS C1 and other germplasm in DCAs20_5629 have better predicted GEBV on average than the TP!

OUTPUT / FILES: everything is in the output/ sub-directory.

DOWNLOAD FROM CASSAVABASE FTP SERVER

or

DOWNLOAD FROM GitHub

Data availability and reproducibility

The R package workflowr was used to document this study reproducibly.

Much of the supporting data and output from the analyses documented here are too large for GitHub.

The repository will be mirrored, here: ftp://ftp.cassavabase.org/marnin_datasets/TARI_2020GS/ with all data.

Directory structure of this repository

NOTICE: data/ and output/ are empty on GitHub. Please see ftp://ftp.cassavabase.org/marnin_datasets/TARI_2020GS/ for access.

  1. data/: raw data (e.g. unimputed SNP data)
  2. output/: outputs (e.g. imputed SNP data)
  3. analysis/: most code and workflow documented in .Rmd files
  4. docs/: compiled .html, “knitted” from .Rmd

Supporting functions code/

The analyses in the html / Rmd files referenced above often source R scripts in the code/ sub-folder.


sessionInfo()
R version 4.0.2 (2020-06-22)
Platform: x86_64-apple-darwin17.0 (64-bit)
Running under: macOS Catalina 10.15.7

Matrix products: default
BLAS:   /Library/Frameworks/R.framework/Versions/4.0/Resources/lib/libRblas.dylib
LAPACK: /Library/Frameworks/R.framework/Versions/4.0/Resources/lib/libRlapack.dylib

locale:
[1] en_US.UTF-8/en_US.UTF-8/en_US.UTF-8/C/en_US.UTF-8/en_US.UTF-8

attached base packages:
[1] stats     graphics  grDevices utils     datasets  methods   base     

other attached packages:
[1] workflowr_1.6.2

loaded via a namespace (and not attached):
 [1] Rcpp_1.0.6      rstudioapi_0.13 whisker_0.4     knitr_1.30     
 [5] magrittr_2.0.1  R6_2.5.0        rlang_0.4.10    stringr_1.4.0  
 [9] tools_4.0.2     xfun_0.20       git2r_0.28.0    htmltools_0.5.1
[13] ellipsis_0.3.1  rprojroot_2.0.2 yaml_2.2.1      digest_0.6.27  
[17] tibble_3.0.5    lifecycle_0.2.0 crayon_1.3.4    later_1.1.0.1  
[21] vctrs_0.3.6     promises_1.1.1  fs_1.5.0        glue_1.4.2     
[25] evaluate_0.14   rmarkdown_2.6   stringi_1.5.3   compiler_4.0.2 
[29] pillar_1.4.7    httpuv_1.5.5    pkgconfig_2.0.3