Comparative Chloroplast Genome Analyses Among Three Sympatric Species of Atraphaxis
DNA was extracted using an improved CTAB method and stored in a refrigerator at -20 ° C. After the DNA samples pass the test, the Covaris ultrasonic crusher is used to randomly break the qualified DNA samples; The preparation of the library was completed through multiple steps such as end repair, ad...
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creator | Zhenzhou Chu Gulibahar Islamu Zezhong Qu Xinmin, Tian |
description | DNA was extracted using an improved CTAB method and stored in a refrigerator at -20 ° C. After the DNA samples pass the test, the Covaris ultrasonic crusher is used to randomly break the qualified DNA samples; The preparation of the library was completed through multiple steps such as end repair, addition of A-tail, addition of sequencing connectors, purification, and PCR amplification; After quality inspection, the Illumina Hiseq 2000 platform of Beijing, China was used to sequence the entire genomes of three species, namely Polygonum spinosum, Polygonum frontalis, and Polygonum slender.
DNA was extracted using an improved CTAB method and stored in a refrigerator at -20 ° C. After the DNA samples pass the test, the Covaris ultrasonic crusher is used to randomly break the qualified DNA samples; The preparation of the library was completed through multiple steps such as end repair, addition of A-tail, addition of sequencing connectors, purification, and PCR amplification; After quality inspection, the Illumina |
doi_str_mv | 10.57760/sciencedb.j00154.00003 |
format | Dataset |
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DNA was extracted using an improved CTAB method and stored in a refrigerator at -20 ° C. After the DNA samples pass the test, the Covaris ultrasonic crusher is used to randomly break the qualified DNA samples; The preparation of the library was completed through multiple steps such as end repair, addition of A-tail, addition of sequencing connectors, purification, and PCR amplification; After quality inspection, the Illumina</description><identifier>DOI: 10.57760/sciencedb.j00154.00003</identifier><language>chi</language><publisher>Science Data Bank</publisher><subject>Atraphaxis ; Biology ; chloroplast genome ; comparative genomics ; phylogeny ; sympatric distribution</subject><creationdate>2023</creationdate><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>776,1887</link.rule.ids><linktorsrc>$$Uhttps://commons.datacite.org/doi.org/10.57760/sciencedb.j00154.00003$$EView_record_in_DataCite.org$$FView_record_in_$$GDataCite.org$$Hfree_for_read</linktorsrc></links><search><creatorcontrib>Zhenzhou Chu</creatorcontrib><creatorcontrib>Gulibahar Islamu</creatorcontrib><creatorcontrib>Zezhong Qu</creatorcontrib><creatorcontrib>Xinmin, Tian</creatorcontrib><title>Comparative Chloroplast Genome Analyses Among Three Sympatric Species of Atraphaxis</title><description>DNA was extracted using an improved CTAB method and stored in a refrigerator at -20 ° C. After the DNA samples pass the test, the Covaris ultrasonic crusher is used to randomly break the qualified DNA samples; The preparation of the library was completed through multiple steps such as end repair, addition of A-tail, addition of sequencing connectors, purification, and PCR amplification; After quality inspection, the Illumina Hiseq 2000 platform of Beijing, China was used to sequence the entire genomes of three species, namely Polygonum spinosum, Polygonum frontalis, and Polygonum slender.
DNA was extracted using an improved CTAB method and stored in a refrigerator at -20 ° C. After the DNA samples pass the test, the Covaris ultrasonic crusher is used to randomly break the qualified DNA samples; The preparation of the library was completed through multiple steps such as end repair, addition of A-tail, addition of sequencing connectors, purification, and PCR amplification; After quality inspection, the Illumina</description><subject>Atraphaxis</subject><subject>Biology</subject><subject>chloroplast genome</subject><subject>comparative genomics</subject><subject>phylogeny</subject><subject>sympatric distribution</subject><fulltext>true</fulltext><rsrctype>dataset</rsrctype><creationdate>2023</creationdate><recordtype>dataset</recordtype><sourceid>PQ8</sourceid><recordid>eNqdzk0OgjAUBOBuXBj1DL4LiCWIrAnxZw_75lkeUtPSpm2M3F6CxgM4m1nN5GNsm_IkL4oj3wepaJDU3pIH52l-SPiUbMnqyhqHHqN6ElS9tt46jSHChQZrCMoB9RgoQGnscIem90RQj9MmeiWhdjQdB7AdlNGj6_GlwpotOtSBNt9eseJ8aqrrrsWIUkUSziuDfhQpFzNP_HjiwxMzL_t_-QZVwE_A</recordid><startdate>20230630</startdate><enddate>20230630</enddate><creator>Zhenzhou Chu</creator><creator>Gulibahar Islamu</creator><creator>Zezhong Qu</creator><creator>Xinmin, Tian</creator><general>Science Data Bank</general><scope>DYCCY</scope><scope>PQ8</scope></search><sort><creationdate>20230630</creationdate><title>Comparative Chloroplast Genome Analyses Among Three Sympatric Species of Atraphaxis</title><author>Zhenzhou Chu ; Gulibahar Islamu ; Zezhong Qu ; Xinmin, Tian</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-datacite_primary_10_57760_sciencedb_j00154_000033</frbrgroupid><rsrctype>datasets</rsrctype><prefilter>datasets</prefilter><language>chi</language><creationdate>2023</creationdate><topic>Atraphaxis</topic><topic>Biology</topic><topic>chloroplast genome</topic><topic>comparative genomics</topic><topic>phylogeny</topic><topic>sympatric distribution</topic><toplevel>online_resources</toplevel><creatorcontrib>Zhenzhou Chu</creatorcontrib><creatorcontrib>Gulibahar Islamu</creatorcontrib><creatorcontrib>Zezhong Qu</creatorcontrib><creatorcontrib>Xinmin, Tian</creatorcontrib><collection>DataCite (Open Access)</collection><collection>DataCite</collection></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext_linktorsrc</fulltext></delivery><addata><au>Zhenzhou Chu</au><au>Gulibahar Islamu</au><au>Zezhong Qu</au><au>Xinmin, Tian</au><format>book</format><genre>unknown</genre><ristype>DATA</ristype><title>Comparative Chloroplast Genome Analyses Among Three Sympatric Species of Atraphaxis</title><date>2023-06-30</date><risdate>2023</risdate><abstract>DNA was extracted using an improved CTAB method and stored in a refrigerator at -20 ° C. After the DNA samples pass the test, the Covaris ultrasonic crusher is used to randomly break the qualified DNA samples; The preparation of the library was completed through multiple steps such as end repair, addition of A-tail, addition of sequencing connectors, purification, and PCR amplification; After quality inspection, the Illumina Hiseq 2000 platform of Beijing, China was used to sequence the entire genomes of three species, namely Polygonum spinosum, Polygonum frontalis, and Polygonum slender.
DNA was extracted using an improved CTAB method and stored in a refrigerator at -20 ° C. After the DNA samples pass the test, the Covaris ultrasonic crusher is used to randomly break the qualified DNA samples; The preparation of the library was completed through multiple steps such as end repair, addition of A-tail, addition of sequencing connectors, purification, and PCR amplification; After quality inspection, the Illumina</abstract><pub>Science Data Bank</pub><doi>10.57760/sciencedb.j00154.00003</doi><oa>free_for_read</oa></addata></record> |
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subjects | Atraphaxis Biology chloroplast genome comparative genomics phylogeny sympatric distribution |
title | Comparative Chloroplast Genome Analyses Among Three Sympatric Species of Atraphaxis |
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