The Development of a High Density Linkage Map for Black Tiger Shrimp
Transcriptome sequencing using Illumina RNA-seq was performed on populations of black tiger shrimp from India. Samples were collected from (i) four landing centres around the east coastline (EC) of India, (ii) survivors of a severe WSSV infection during pond culture (SUR) and (iii) the Andaman Islan...
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creator | Baranski, Matthew Gopikrishna, Gopalapillay Robinson, Nicholas A Katneni, Vinaya Kumar Shekhar, Mudagandur S Shanmugakarthik, Jayakani Jothivel, Sarangapani Gopal, Chavali Ravichandran, Pitchaiyappan Kent, Matthew Arnyasi, Mariann Ponniah, Alphis G |
description | Transcriptome sequencing using Illumina RNA-seq was performed on populations of black tiger shrimp from India. Samples were collected from (i) four landing centres around the east coastline (EC) of India, (ii) survivors of a severe WSSV infection during pond culture (SUR) and (iii) the Andaman Islands (AI) in the Bay of Bengal. Equal quantities of purified total RNA from homogenates of hepatopancreas, muscle, nervous tissue, intestinal tract, heart, gonad, gills, pleopod and lymphoid organs were combined to create AI, EC and SUR pools for RNA sequencing. De novo transcriptome assembly resulted in 136,223 contigs (minimum size 100 base pairs, bp) with a total length 61 Mb, an average length of 446 bp and an average coverage of 163x across all pools. Approximately 16% of contigs were annotated with BLAST hit information and gene ontology annotations. A total of 473,620 putative SNPs/indels were identified. An Illumina iSelect genotyping array containing 6,000 SNPs was developed and used to genotype 1024 offspring belonging to seven full-sibling families. A total of 3959 SNPs were mapped to 44 linkage groups. The linkage groups consisted of between 16-129 and 13-130 markers, of length between 139-10.8 and 109.1-10.5 cM and with intervals averaging between 1.2 and 0.9 cM for the female and male maps respectively. The female map was 28% longer than the male map (4060 and 2917 cM respectively) with a 1.6 higher recombination rate observed for female compared to male meioses. This approach has substantially increased expressed sequence and DNA marker resources for tiger shrimp and is a useful resource for QTL mapping and association studies for evolutionarily and commercially important traits. |
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Samples were collected from (i) four landing centres around the east coastline (EC) of India, (ii) survivors of a severe WSSV infection during pond culture (SUR) and (iii) the Andaman Islands (AI) in the Bay of Bengal. Equal quantities of purified total RNA from homogenates of hepatopancreas, muscle, nervous tissue, intestinal tract, heart, gonad, gills, pleopod and lymphoid organs were combined to create AI, EC and SUR pools for RNA sequencing. De novo transcriptome assembly resulted in 136,223 contigs (minimum size 100 base pairs, bp) with a total length 61 Mb, an average length of 446 bp and an average coverage of 163x across all pools. Approximately 16% of contigs were annotated with BLAST hit information and gene ontology annotations. A total of 473,620 putative SNPs/indels were identified. An Illumina iSelect genotyping array containing 6,000 SNPs was developed and used to genotype 1024 offspring belonging to seven full-sibling families. A total of 3959 SNPs were mapped to 44 linkage groups. The linkage groups consisted of between 16-129 and 13-130 markers, of length between 139-10.8 and 109.1-10.5 cM and with intervals averaging between 1.2 and 0.9 cM for the female and male maps respectively. The female map was 28% longer than the male map (4060 and 2917 cM respectively) with a 1.6 higher recombination rate observed for female compared to male meioses. 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Samples were collected from (i) four landing centres around the east coastline (EC) of India, (ii) survivors of a severe WSSV infection during pond culture (SUR) and (iii) the Andaman Islands (AI) in the Bay of Bengal. Equal quantities of purified total RNA from homogenates of hepatopancreas, muscle, nervous tissue, intestinal tract, heart, gonad, gills, pleopod and lymphoid organs were combined to create AI, EC and SUR pools for RNA sequencing. De novo transcriptome assembly resulted in 136,223 contigs (minimum size 100 base pairs, bp) with a total length 61 Mb, an average length of 446 bp and an average coverage of 163x across all pools. Approximately 16% of contigs were annotated with BLAST hit information and gene ontology annotations. A total of 473,620 putative SNPs/indels were identified. An Illumina iSelect genotyping array containing 6,000 SNPs was developed and used to genotype 1024 offspring belonging to seven full-sibling families. A total of 3959 SNPs were mapped to 44 linkage groups. The linkage groups consisted of between 16-129 and 13-130 markers, of length between 139-10.8 and 109.1-10.5 cM and with intervals averaging between 1.2 and 0.9 cM for the female and male maps respectively. The female map was 28% longer than the male map (4060 and 2917 cM respectively) with a 1.6 higher recombination rate observed for female compared to male meioses. This approach has substantially increased expressed sequence and DNA marker resources for tiger shrimp and is a useful resource for QTL mapping and association studies for evolutionarily and commercially important traits.</description><subject>Genes</subject><subject>Genetic markers</subject><subject>Health aspects</subject><subject>Quantitative genetics</subject><subject>RNA</subject><subject>RNA sequencing</subject><issn>1932-6203</issn><issn>1932-6203</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2014</creationdate><recordtype>article</recordtype><recordid>eNqFzEFLwzAcBfAgCs7pN_CQk-ChM1maNDnOTd1gMnDF60jbf9psWVKaTvTbO9DDPHl6j8ePh9AtJSPKMvqwDYfOazdqg4cRIZKnlJ2hAVVsnIgxYecn_RJdxbglhDMpxADN8gbwDD7AhXYPvsfBYI3ntm6Oq4-2_8JL63e6BvyqW2xChx-dLnc4tzV0eN10dt9eowujXYSb3xyi_Pkpn86T5eplMZ0sk1opnqRMZaBKRUUGhipRMU2qVBupSVEyIbgkJUhVEmOklMU4rdKCcJEdnSm4rtgQ3f_c1trBxvoy-B4--1ofYtws1m-bSZpJKaji_B-7ev9r705sA9r1TQzu0Nvg4yn8BlAaawU</recordid><startdate>20140117</startdate><enddate>20140117</enddate><creator>Baranski, Matthew</creator><creator>Gopikrishna, Gopalapillay</creator><creator>Robinson, Nicholas A</creator><creator>Katneni, Vinaya Kumar</creator><creator>Shekhar, Mudagandur S</creator><creator>Shanmugakarthik, Jayakani</creator><creator>Jothivel, Sarangapani</creator><creator>Gopal, Chavali</creator><creator>Ravichandran, Pitchaiyappan</creator><creator>Kent, Matthew</creator><creator>Arnyasi, Mariann</creator><creator>Ponniah, Alphis G</creator><general>Public Library of Science</general><scope>IOV</scope><scope>ISR</scope></search><sort><creationdate>20140117</creationdate><title>The Development of a High Density Linkage Map for Black Tiger Shrimp</title><author>Baranski, Matthew ; Gopikrishna, Gopalapillay ; Robinson, Nicholas A ; Katneni, Vinaya Kumar ; Shekhar, Mudagandur S ; Shanmugakarthik, Jayakani ; Jothivel, Sarangapani ; Gopal, Chavali ; Ravichandran, Pitchaiyappan ; Kent, Matthew ; Arnyasi, Mariann ; Ponniah, Alphis G</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-g995-4397e9c9167ef196d3a0d4af8a0bc366580ce89c0ff888b24d4b0567d3afb5ad3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2014</creationdate><topic>Genes</topic><topic>Genetic markers</topic><topic>Health aspects</topic><topic>Quantitative genetics</topic><topic>RNA</topic><topic>RNA sequencing</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Baranski, Matthew</creatorcontrib><creatorcontrib>Gopikrishna, Gopalapillay</creatorcontrib><creatorcontrib>Robinson, Nicholas A</creatorcontrib><creatorcontrib>Katneni, Vinaya Kumar</creatorcontrib><creatorcontrib>Shekhar, Mudagandur S</creatorcontrib><creatorcontrib>Shanmugakarthik, Jayakani</creatorcontrib><creatorcontrib>Jothivel, Sarangapani</creatorcontrib><creatorcontrib>Gopal, Chavali</creatorcontrib><creatorcontrib>Ravichandran, Pitchaiyappan</creatorcontrib><creatorcontrib>Kent, Matthew</creatorcontrib><creatorcontrib>Arnyasi, Mariann</creatorcontrib><creatorcontrib>Ponniah, Alphis G</creatorcontrib><collection>Gale In Context: Opposing Viewpoints</collection><collection>Gale In Context: Science</collection><jtitle>PloS one</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Baranski, Matthew</au><au>Gopikrishna, Gopalapillay</au><au>Robinson, Nicholas A</au><au>Katneni, Vinaya Kumar</au><au>Shekhar, Mudagandur S</au><au>Shanmugakarthik, Jayakani</au><au>Jothivel, Sarangapani</au><au>Gopal, Chavali</au><au>Ravichandran, Pitchaiyappan</au><au>Kent, Matthew</au><au>Arnyasi, Mariann</au><au>Ponniah, Alphis G</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>The Development of a High Density Linkage Map for Black Tiger Shrimp</atitle><jtitle>PloS one</jtitle><date>2014-01-17</date><risdate>2014</risdate><volume>9</volume><issue>1</issue><spage>e85413</spage><pages>e85413-</pages><issn>1932-6203</issn><eissn>1932-6203</eissn><abstract>Transcriptome sequencing using Illumina RNA-seq was performed on populations of black tiger shrimp from India. Samples were collected from (i) four landing centres around the east coastline (EC) of India, (ii) survivors of a severe WSSV infection during pond culture (SUR) and (iii) the Andaman Islands (AI) in the Bay of Bengal. Equal quantities of purified total RNA from homogenates of hepatopancreas, muscle, nervous tissue, intestinal tract, heart, gonad, gills, pleopod and lymphoid organs were combined to create AI, EC and SUR pools for RNA sequencing. De novo transcriptome assembly resulted in 136,223 contigs (minimum size 100 base pairs, bp) with a total length 61 Mb, an average length of 446 bp and an average coverage of 163x across all pools. Approximately 16% of contigs were annotated with BLAST hit information and gene ontology annotations. A total of 473,620 putative SNPs/indels were identified. An Illumina iSelect genotyping array containing 6,000 SNPs was developed and used to genotype 1024 offspring belonging to seven full-sibling families. A total of 3959 SNPs were mapped to 44 linkage groups. The linkage groups consisted of between 16-129 and 13-130 markers, of length between 139-10.8 and 109.1-10.5 cM and with intervals averaging between 1.2 and 0.9 cM for the female and male maps respectively. The female map was 28% longer than the male map (4060 and 2917 cM respectively) with a 1.6 higher recombination rate observed for female compared to male meioses. This approach has substantially increased expressed sequence and DNA marker resources for tiger shrimp and is a useful resource for QTL mapping and association studies for evolutionarily and commercially important traits.</abstract><pub>Public Library of Science</pub><doi>10.1371/journal.pone.0085413</doi><tpages>e85413</tpages></addata></record> |
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title | The Development of a High Density Linkage Map for Black Tiger Shrimp |
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