seqminer (Q31506)

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Efficiently Read Sequence Data (VCF Format, BCF Format, METAL Format and BGEN Format) into R
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seqminer
Efficiently Read Sequence Data (VCF Format, BCF Format, METAL Format and BGEN Format) into R

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    8.9
    7 April 2023
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    0.1
    20 March 2013
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    0.2
    1 April 2013
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    0.3
    13 April 2013
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    0.5
    28 May 2013
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    0.7
    29 July 2013
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    1.0
    4 September 2013
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    1.3
    26 September 2013
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    1.4
    29 September 2013
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    1.9.1
    15 November 2013
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    1.9
    11 November 2013
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    2.0
    20 November 2013
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    2.2
    27 January 2014
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    2.7
    14 April 2014
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    3.0
    19 April 2014
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    3.1
    7 May 2014
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    3.4
    8 December 2014
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    3.7
    16 May 2015
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    3.9
    21 May 2015
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    4.2
    10 June 2015
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    4.5
    29 June 2015
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    4.7
    19 August 2015
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    4.9
    16 September 2015
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    5.0
    22 October 2015
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    5.2
    3 May 2016
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    5.3
    7 May 2016
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    5.7
    13 January 2017
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    5.9
    18 April 2017
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    6.0
    5 May 2017
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    6.1
    2 August 2018
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    6.7
    6 December 2018
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    7.0
    7 January 2019
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    7.1
    8 January 2019
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    8.0
    2 March 2020
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    8.2
    9 November 2021
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    8.4
    7 February 2022
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    8.5
    15 November 2022
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    8.6
    26 January 2023
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    9.1
    2 September 2023
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    9.3
    28 November 2023
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    9.4
    3 February 2024
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    3 February 2024
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    Integrate sequencing data (Variant call format, e.g. VCF or BCF) or meta-analysis results in R. This package can help you (1) read VCF/BCF/BGEN files by chromosomal ranges (e.g. 1:100-200); (2) read RareMETAL summary statistics files; (3) read tables from a tabix-indexed files; (4) annotate VCF/BCF files; (5) create customized workflow based on Makefile.
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