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Update seqBlockApply.Rd
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man/seqBlockApply.Rd

Lines changed: 11 additions & 5 deletions
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@@ -69,21 +69,27 @@ associated with these variables.
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\code{"$dosage_alt"} returns a RAW/INTEGER matrix for the dosages of alternative
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allele without distinguishing different alternative alleles.
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\code{"$dosage_alt2"} allow the alleles are partially missing (e.g., genotypes
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on chromosome X for males)
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\code{"$dosage_sp"} returns a sparse matrix (dgCMatrix) for the dosages of
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alternative allele without distinguishing different alternative alleles.
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\code{"$dosage_sp2"} allow the alleles are partially missing (e.g., genotypes
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on chromosome X for males)
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\code{"$num_allele"} returns an integer vector with the numbers of distinct
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alleles.
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\code{"$ref"} returns a character vector of reference alleles
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\code{"$ref"} returns a character vector of reference alleles.
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\code{"$alt"} returns a character vector of alternative alleles (delimited by
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comma)
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comma).
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\code{"$chrom_pos"} returns characters with the combination of chromosome and
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position, e.g., "1:1272721". \code{"$chrom_pos_allele"} returns characters with
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the combination of chromosome, position and alleles, e.g., "1:1272721_A_G"
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position, e.g., "1:1272721". \code{"$chrom_pos2"} is similar to
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\code{"$chrom_pos"}, except the suffix "_1" is added to the first duplicate
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following the variant, "_2" is added to the second duplicate, and so on.
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\code{"$chrom_pos_allele"} returns characters with the combination of
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chromosome, position and alleles, e.g., "1:1272721_A_G"
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(i.e., chr:position_REF_ALT).
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\code{"$variant_index"} returns the indices of selected variants starting

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