full_merge {minSNPs} | R Documentation |
full_merge
Description
full_merge
is used to merge 2 fasta,
where a position exist only in 1 of the fasta, the fasta without allele
in that positions are given reference genome's allele at that position.
**Doesn't work for large dataset, hence the need for full_merge_1
**
Usage
full_merge(
fasta_1,
fasta_2,
meta_1,
meta_2,
ref,
bp = BiocParallel::MulticoreParam(),
...
)
Arguments
fasta_1 |
fasta read into memory to join |
fasta_2 |
fasta read into memory to join |
meta_1 |
meta file for 'fasta_1' denoting all positions of SNPs and position in reference genome |
meta_2 |
meta file for 'fasta_2' denoting all positions of SNPs and position in reference genome |
ref |
name of the reference genome (needs to be in both fasta files) |
bp |
the BiocParallel backend |
... |
all other arguments |
Value
merged fasta and meta
[Package minSNPs version 0.2.0 Index]