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zhanxw committed Sep 30, 2024
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4 changes: 4 additions & 0 deletions ChangeLog
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2024-09-30 Xiaowei Zhan <[email protected]>

* Revise URL used in README

2024-09-24 Xiaowei Zhan <[email protected]>

* Add R_NO_REMAP to better support calling R API for C codes
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4 changes: 2 additions & 2 deletions DESCRIPTION
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Expand Up @@ -2,8 +2,8 @@ Package: seqminer
Type: Package
Title: Efficiently Read Sequence Data (VCF Format, BCF Format, METAL
Format and BGEN Format) into R
Version: 9.5
Date: 2024-09-24
Version: 9.6
Date: 2024-09-30
Authors@R: c(person("Xiaowei", "Zhan", email = "[email protected]", role = c("aut", "cre")),
person("Dajiang", "Liu", email = "[email protected]", role = "aut"),
person("Attractive Chaos", email = "[email protected]", role = "cph", comment = "We have used the following software and made minimal necessary changes: Tabix, Heng Li <[email protected]> (MIT license). We removed standard IO related functions, e.g. printf, fprintf ; also changed its un-safe pointer arithmetics."),
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2 changes: 1 addition & 1 deletion README.md
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Expand Up @@ -87,6 +87,6 @@ We also developed a seqminer command line interface:

Citation:

[Yang, L., Jiang, S., Jiang, B., Liu, D. J., & Zhan, X. (2020). Seqminer2: An Efficient Tool to Query and Retrieve Genotypes for Statistical Genetics Analyses from Biobank Scale Sequence Dataset. Bioinformatics](https://academic.oup.com/bioinformatics/advance-article-abstract/doi/10.1093/bioinformatics/btaa628/5881355?redirectedFrom=fulltext)
[Yang, L., Jiang, S., Jiang, B., Liu, D. J., & Zhan, X. (2020). Seqminer2: An Efficient Tool to Query and Retrieve Genotypes for Statistical Genetics Analyses from Biobank Scale Sequence Dataset. Bioinformatics](https://doi.org/10.1093/bioinformatics/btaa628)

[Zhan, X. and Liu, D. J. (2015), SEQMINER: An R-Package to Facilitate the Functional Interpretation of Sequence-Based Associations. Genet. Epidemiol., 39: 619–623. doi:10.1002/gepi.21918](https://doi.org/10.1002/gepi.21918)

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