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-rw-r--r--doc/code/pangemma.md3
1 files changed, 1 insertions, 2 deletions
diff --git a/doc/code/pangemma.md b/doc/code/pangemma.md
index 1c3fed9..91d877c 100644
--- a/doc/code/pangemma.md
+++ b/doc/code/pangemma.md
@@ -246,10 +246,9 @@ Alright, to duplicate above filtering routine we are going to add an alternative
read-geno-file (with filtering) -> list-of-filtered-genotypes
rb-read-geno-file -> rb-filter-geno-file -> ''
-'read-geno-file' translates to GEMMA's read-geno-file and rb-read-geno-file is the alternate path. list-of-filtered-genotypes will be a file that we can compare between the two paths.
+'read-geno-file' translates to GEMMA's read-geno-file (maybe I should name it gemma-read-geno-file) and rb-read-geno-file is the alternate path. list-of-filtered-genotypes will be a file that we can compare between the two paths.
These steps should be so simple that anyone can replace them with, say, a python version. So, what can go wrong?
-
# Other
## Example