SRX2594160 CEME MAR1-1 02Jan2014 L004 SRP055973 PRJNA275988 Double-digest RADseq using PstI on the forward (R1) end and MseI on the reverse (R2). Barcodes of 6bp length were incorporated into the adapters on both ends and were removed during de-multiplexing of the samples. Fragments of 350-650 bp were size selected with a Pippin Prep. Sequencing was 100bp paired-end Illumina HiSeq 2000. SRS868511 SAMN03377072 CEME MAR1-1 02Jan2014 L004 OTHER GENOMIC Reduced Representation Illumina HiSeq 2000 SRX2594161 CEME MAR1-1 02Jan2014 L003 SRP055973 PRJNA275988 Double-digest RADseq using PstI on the forward (R1) end and MseI on the reverse (R2). Barcodes of 6bp length were incorporated into the adapters on both ends and were removed during de-multiplexing of the samples. Fragments of 350-650 bp were size selected with a Pippin Prep. Sequencing was 100bp paired-end Illumina HiSeq 2000. SRS868511 SAMN03377072 CEME MAR1-1 02Jan2014 L003 OTHER GENOMIC Reduced Representation Illumina HiSeq 2000 SRX2594162 CEME COA3-1 16May2014 L007 SRP055973 PRJNA275988 Double-digest RADseq using PstI on the forward (R1) end and MseI on the reverse (R2). Barcodes of 6bp length were incorporated into the adapters on both ends and were removed during de-multiplexing of the samples. Fragments of 350-650 bp were size selected with a Pippin Prep. Sequencing was 100bp paired-end Illumina HiSeq 2000. SRS868257 SAMN03377079 CEME COA3-1 16May2014 L007 OTHER GENOMIC Reduced Representation Illumina HiSeq 2000 SRX2594163 CEME CAL2-1 16May2014 L007 SRP055973 PRJNA275988 Double-digest RADseq using PstI on the forward (R1) end and MseI on the reverse (R2). Barcodes of 6bp length were incorporated into the adapters on both ends and were removed during de-multiplexing of the samples. Fragments of 350-650 bp were size selected with a Pippin Prep. Sequencing was 100bp paired-end Illumina HiSeq 2000. SRS868510 SAMN03377078 CEME CAL2-1 16May2014 L007 OTHER GENOMIC Reduced Representation Illumina HiSeq 2000