ERX1417576 ena-EXPERIMENT-ROSLIN INSTITUTE, UNIVERSITY OF EDINBURGH-01-04-2016-11:45:44:781-1 ERP014795 2kb size selected ERS1101127 SAMEA3913993 J-line Chickens Brain Isoseq 1 OTHER TRANSCRIPTOMIC other Brain tissue from J-line chickens was collected and RNA was extracted. The RNA was selected for poly-A tails. Normalization by denature/renature was applied to synthesized cDNA. The cDNA were then size selected for 1kb and 2kb lengths using Ampure beads. For the 1kb cDNA, 11 SMRT cells were used. For the 2kb cDNA, 14 SMRT cells were used. Sequencing was performed on an RSII Pacific Biosciences machine using P4C2 chemistry. PacBio RS ERX1417577 ena-EXPERIMENT-ROSLIN INSTITUTE, UNIVERSITY OF EDINBURGH-01-04-2016-11:45:44:781-2 ERP014795 2kb size selected ERS1101128 SAMEA3913994 J-line Chickens Brain Isoseq 2 OTHER TRANSCRIPTOMIC other Brain tissue from J-line chickens was collected and RNA was extracted. The RNA was selected for poly-A tails. Normalization by denature/renature was applied to synthesized cDNA. The cDNA were then size selected for 1kb and 2kb lengths using Ampure beads. For the 1kb cDNA, 11 SMRT cells were used. For the 2kb cDNA, 14 SMRT cells were used. Sequencing was performed on an RSII Pacific Biosciences machine using P4C2 chemistry. PacBio RS ERX1417578 ena-EXPERIMENT-ROSLIN INSTITUTE, UNIVERSITY OF EDINBURGH-01-04-2016-11:45:44:781-3 ERP014795 2kb size selected ERS1101129 SAMEA3913995 J-line Chickens Brain Isoseq 3 OTHER TRANSCRIPTOMIC other Brain tissue from J-line chickens was collected and RNA was extracted. The RNA was selected for poly-A tails. Normalization by denature/renature was applied to synthesized cDNA. The cDNA were then size selected for 1kb and 2kb lengths using Ampure beads. For the 1kb cDNA, 11 SMRT cells were used. For the 2kb cDNA, 14 SMRT cells were used. Sequencing was performed on an RSII Pacific Biosciences machine using P4C2 chemistry. PacBio RS ERX1417579 ena-EXPERIMENT-ROSLIN INSTITUTE, UNIVERSITY OF EDINBURGH-01-04-2016-11:45:44:781-4 ERP014795 2kb size selected ERS1101130 SAMEA3913996 J-line Chickens Brain Isoseq 4 OTHER TRANSCRIPTOMIC other Brain tissue from J-line chickens was collected and RNA was extracted. The RNA was selected for poly-A tails. Normalization by denature/renature was applied to synthesized cDNA. The cDNA were then size selected for 1kb and 2kb lengths using Ampure beads. For the 1kb cDNA, 11 SMRT cells were used. For the 2kb cDNA, 14 SMRT cells were used. Sequencing was performed on an RSII Pacific Biosciences machine using P4C2 chemistry. PacBio RS ERX1417580 ena-EXPERIMENT-ROSLIN INSTITUTE, UNIVERSITY OF EDINBURGH-01-04-2016-11:45:44:781-5 ERP014795 2kb size selected ERS1101131 SAMEA3913997 J-line Chickens Brain Isoseq 5 OTHER TRANSCRIPTOMIC other Brain tissue from J-line chickens was collected and RNA was extracted. The RNA was selected for poly-A tails. Normalization by denature/renature was applied to synthesized cDNA. The cDNA were then size selected for 1kb and 2kb lengths using Ampure beads. For the 1kb cDNA, 11 SMRT cells were used. For the 2kb cDNA, 14 SMRT cells were used. Sequencing was performed on an RSII Pacific Biosciences machine using P4C2 chemistry. PacBio RS ERX1417581 ena-EXPERIMENT-ROSLIN INSTITUTE, UNIVERSITY OF EDINBURGH-01-04-2016-11:45:44:781-6 ERP014795 2kb size selected ERS1101132 SAMEA3913998 J-line Chickens Brain Isoseq 6 OTHER TRANSCRIPTOMIC other Brain tissue from J-line chickens was collected and RNA was extracted. The RNA was selected for poly-A tails. Normalization by denature/renature was applied to synthesized cDNA. The cDNA were then size selected for 1kb and 2kb lengths using Ampure beads. For the 1kb cDNA, 11 SMRT cells were used. For the 2kb cDNA, 14 SMRT cells were used. Sequencing was performed on an RSII Pacific Biosciences machine using P4C2 chemistry. PacBio RS ERX1417582 ena-EXPERIMENT-ROSLIN INSTITUTE, UNIVERSITY OF EDINBURGH-01-04-2016-11:45:44:782-7 ERP014795 2kb size selected ERS1101133 SAMEA3913999 J-line Chickens Brain Isoseq 7 OTHER TRANSCRIPTOMIC other Brain tissue from J-line chickens was collected and RNA was extracted. The RNA was selected for poly-A tails. Normalization by denature/renature was applied to synthesized cDNA. The cDNA were then size selected for 1kb and 2kb lengths using Ampure beads. For the 1kb cDNA, 11 SMRT cells were used. For the 2kb cDNA, 14 SMRT cells were used. Sequencing was performed on an RSII Pacific Biosciences machine using P4C2 chemistry. PacBio RS ERX1417583 ena-EXPERIMENT-ROSLIN INSTITUTE, UNIVERSITY OF EDINBURGH-01-04-2016-11:45:44:782-8 ERP014795 2kb size selected ERS1101134 SAMEA3914000 J-line Chickens Brain Isoseq 8 OTHER TRANSCRIPTOMIC other Brain tissue from J-line chickens was collected and RNA was extracted. The RNA was selected for poly-A tails. Normalization by denature/renature was applied to synthesized cDNA. The cDNA were then size selected for 1kb and 2kb lengths using Ampure beads. For the 1kb cDNA, 11 SMRT cells were used. For the 2kb cDNA, 14 SMRT cells were used. Sequencing was performed on an RSII Pacific Biosciences machine using P4C2 chemistry. PacBio RS ERX1417584 ena-EXPERIMENT-ROSLIN INSTITUTE, UNIVERSITY OF EDINBURGH-01-04-2016-11:45:44:782-9 ERP014795 2kb size selected ERS1101135 SAMEA3914001 J-line Chickens Brain Isoseq 9 OTHER TRANSCRIPTOMIC other Brain tissue from J-line chickens was collected and RNA was extracted. The RNA was selected for poly-A tails. Normalization by denature/renature was applied to synthesized cDNA. The cDNA were then size selected for 1kb and 2kb lengths using Ampure beads. For the 1kb cDNA, 11 SMRT cells were used. For the 2kb cDNA, 14 SMRT cells were used. Sequencing was performed on an RSII Pacific Biosciences machine using P4C2 chemistry. PacBio RS ERX1417585 ena-EXPERIMENT-ROSLIN INSTITUTE, UNIVERSITY OF EDINBURGH-01-04-2016-11:45:44:782-10 ERP014795 2kb size selected ERS1101136 SAMEA3914002 J-line Chickens Brain Isoseq 10 OTHER TRANSCRIPTOMIC other Brain tissue from J-line chickens was collected and RNA was extracted. The RNA was selected for poly-A tails. Normalization by denature/renature was applied to synthesized cDNA. The cDNA were then size selected for 1kb and 2kb lengths using Ampure beads. For the 1kb cDNA, 11 SMRT cells were used. For the 2kb cDNA, 14 SMRT cells were used. Sequencing was performed on an RSII Pacific Biosciences machine using P4C2 chemistry. PacBio RS ERX1417586 ena-EXPERIMENT-ROSLIN INSTITUTE, UNIVERSITY OF EDINBURGH-01-04-2016-11:45:44:782-11 ERP014795 2kb size selected ERS1101137 SAMEA3914003 J-line Chickens Brain Isoseq 11 OTHER TRANSCRIPTOMIC other Brain tissue from J-line chickens was collected and RNA was extracted. The RNA was selected for poly-A tails. Normalization by denature/renature was applied to synthesized cDNA. The cDNA were then size selected for 1kb and 2kb lengths using Ampure beads. For the 1kb cDNA, 11 SMRT cells were used. For the 2kb cDNA, 14 SMRT cells were used. Sequencing was performed on an RSII Pacific Biosciences machine using P4C2 chemistry. PacBio RS ERX1417587 ena-EXPERIMENT-ROSLIN INSTITUTE, UNIVERSITY OF EDINBURGH-01-04-2016-11:45:44:782-12 ERP014795 2kb size selected ERS1101138 SAMEA3914004 J-line Chickens Brain Isoseq 12 OTHER TRANSCRIPTOMIC other Brain tissue from J-line chickens was collected and RNA was extracted. The RNA was selected for poly-A tails. Normalization by denature/renature was applied to synthesized cDNA. The cDNA were then size selected for 1kb and 2kb lengths using Ampure beads. For the 1kb cDNA, 11 SMRT cells were used. For the 2kb cDNA, 14 SMRT cells were used. Sequencing was performed on an RSII Pacific Biosciences machine using P4C2 chemistry. PacBio RS ERX1417588 ena-EXPERIMENT-ROSLIN INSTITUTE, UNIVERSITY OF EDINBURGH-01-04-2016-11:45:44:782-13 ERP014795 2kb size selected ERS1101139 SAMEA3914005 J-line Chickens Brain Isoseq 13 OTHER TRANSCRIPTOMIC other Brain tissue from J-line chickens was collected and RNA was extracted. The RNA was selected for poly-A tails. Normalization by denature/renature was applied to synthesized cDNA. The cDNA were then size selected for 1kb and 2kb lengths using Ampure beads. For the 1kb cDNA, 11 SMRT cells were used. For the 2kb cDNA, 14 SMRT cells were used. Sequencing was performed on an RSII Pacific Biosciences machine using P4C2 chemistry. PacBio RS ERX1417589 ena-EXPERIMENT-ROSLIN INSTITUTE, UNIVERSITY OF EDINBURGH-01-04-2016-11:45:44:782-14 ERP014795 2kb size selected ERS1101140 SAMEA3914006 J-line Chickens Brain Isoseq 14 OTHER TRANSCRIPTOMIC other Brain tissue from J-line chickens was collected and RNA was extracted. The RNA was selected for poly-A tails. Normalization by denature/renature was applied to synthesized cDNA. The cDNA were then size selected for 1kb and 2kb lengths using Ampure beads. For the 1kb cDNA, 11 SMRT cells were used. For the 2kb cDNA, 14 SMRT cells were used. Sequencing was performed on an RSII Pacific Biosciences machine using P4C2 chemistry. PacBio RS ERX1417590 ena-EXPERIMENT-ROSLIN INSTITUTE, UNIVERSITY OF EDINBURGH-01-04-2016-11:45:44:782-15 ERP014795 1kb size selected ERS1101141 SAMEA3914007 J-line Chickens Brain Isoseq 15 OTHER TRANSCRIPTOMIC other Brain tissue from J-line chickens was collected and RNA was extracted. The RNA was selected for poly-A tails. Normalization by denature/renature was applied to synthesized cDNA. The cDNA were then size selected for 1kb and 2kb lengths using Ampure beads. For the 1kb cDNA, 11 SMRT cells were used. For the 2kb cDNA, 14 SMRT cells were used. Sequencing was performed on an RSII Pacific Biosciences machine using P4C2 chemistry. PacBio RS ERX1417591 ena-EXPERIMENT-ROSLIN INSTITUTE, UNIVERSITY OF EDINBURGH-01-04-2016-11:45:44:782-16 ERP014795 1kb size selected ERS1101142 SAMEA3914008 J-line Chickens Brain Isoseq 16 OTHER TRANSCRIPTOMIC other Brain tissue from J-line chickens was collected and RNA was extracted. The RNA was selected for poly-A tails. Normalization by denature/renature was applied to synthesized cDNA. The cDNA were then size selected for 1kb and 2kb lengths using Ampure beads. For the 1kb cDNA, 11 SMRT cells were used. For the 2kb cDNA, 14 SMRT cells were used. Sequencing was performed on an RSII Pacific Biosciences machine using P4C2 chemistry. PacBio RS ERX1417592 ena-EXPERIMENT-ROSLIN INSTITUTE, UNIVERSITY OF EDINBURGH-01-04-2016-11:45:44:782-17 ERP014795 1kb size selected ERS1101143 SAMEA3914009 J-line Chickens Brain Isoseq 17 OTHER TRANSCRIPTOMIC other Brain tissue from J-line chickens was collected and RNA was extracted. The RNA was selected for poly-A tails. Normalization by denature/renature was applied to synthesized cDNA. The cDNA were then size selected for 1kb and 2kb lengths using Ampure beads. For the 1kb cDNA, 11 SMRT cells were used. For the 2kb cDNA, 14 SMRT cells were used. Sequencing was performed on an RSII Pacific Biosciences machine using P4C2 chemistry. PacBio RS ERX1417593 ena-EXPERIMENT-ROSLIN INSTITUTE, UNIVERSITY OF EDINBURGH-01-04-2016-11:45:44:782-18 ERP014795 1kb size selected ERS1101144 SAMEA3914010 J-line Chickens Brain Isoseq 18 OTHER TRANSCRIPTOMIC other Brain tissue from J-line chickens was collected and RNA was extracted. The RNA was selected for poly-A tails. Normalization by denature/renature was applied to synthesized cDNA. The cDNA were then size selected for 1kb and 2kb lengths using Ampure beads. For the 1kb cDNA, 11 SMRT cells were used. For the 2kb cDNA, 14 SMRT cells were used. Sequencing was performed on an RSII Pacific Biosciences machine using P4C2 chemistry. PacBio RS ERX1417594 ena-EXPERIMENT-ROSLIN INSTITUTE, UNIVERSITY OF EDINBURGH-01-04-2016-11:45:44:783-19 ERP014795 1kb size selected ERS1101145 SAMEA3914011 J-line Chickens Brain Isoseq 19 OTHER TRANSCRIPTOMIC other Brain tissue from J-line chickens was collected and RNA was extracted. The RNA was selected for poly-A tails. Normalization by denature/renature was applied to synthesized cDNA. The cDNA were then size selected for 1kb and 2kb lengths using Ampure beads. For the 1kb cDNA, 11 SMRT cells were used. For the 2kb cDNA, 14 SMRT cells were used. Sequencing was performed on an RSII Pacific Biosciences machine using P4C2 chemistry. PacBio RS ERX1417595 ena-EXPERIMENT-ROSLIN INSTITUTE, UNIVERSITY OF EDINBURGH-01-04-2016-11:45:44:783-20 ERP014795 1kb size selected ERS1101146 SAMEA3914012 J-line Chickens Brain Isoseq 20 OTHER TRANSCRIPTOMIC other Brain tissue from J-line chickens was collected and RNA was extracted. The RNA was selected for poly-A tails. Normalization by denature/renature was applied to synthesized cDNA. The cDNA were then size selected for 1kb and 2kb lengths using Ampure beads. For the 1kb cDNA, 11 SMRT cells were used. For the 2kb cDNA, 14 SMRT cells were used. Sequencing was performed on an RSII Pacific Biosciences machine using P4C2 chemistry. PacBio RS ERX1417596 ena-EXPERIMENT-ROSLIN INSTITUTE, UNIVERSITY OF EDINBURGH-01-04-2016-11:45:44:783-21 ERP014795 1kb size selected ERS1101147 SAMEA3914013 J-line Chickens Brain Isoseq 21 OTHER TRANSCRIPTOMIC other Brain tissue from J-line chickens was collected and RNA was extracted. The RNA was selected for poly-A tails. Normalization by denature/renature was applied to synthesized cDNA. The cDNA were then size selected for 1kb and 2kb lengths using Ampure beads. For the 1kb cDNA, 11 SMRT cells were used. For the 2kb cDNA, 14 SMRT cells were used. Sequencing was performed on an RSII Pacific Biosciences machine using P4C2 chemistry. PacBio RS ERX1417597 ena-EXPERIMENT-ROSLIN INSTITUTE, UNIVERSITY OF EDINBURGH-01-04-2016-11:45:44:783-22 ERP014795 1kb size selected ERS1101148 SAMEA3914014 J-line Chickens Brain Isoseq 22 OTHER TRANSCRIPTOMIC other Brain tissue from J-line chickens was collected and RNA was extracted. The RNA was selected for poly-A tails. Normalization by denature/renature was applied to synthesized cDNA. The cDNA were then size selected for 1kb and 2kb lengths using Ampure beads. For the 1kb cDNA, 11 SMRT cells were used. For the 2kb cDNA, 14 SMRT cells were used. Sequencing was performed on an RSII Pacific Biosciences machine using P4C2 chemistry. PacBio RS ERX1417598 ena-EXPERIMENT-ROSLIN INSTITUTE, UNIVERSITY OF EDINBURGH-01-04-2016-11:45:44:783-23 ERP014795 1kb size selected ERS1101149 SAMEA3914015 J-line Chickens Brain Isoseq 23 OTHER TRANSCRIPTOMIC other Brain tissue from J-line chickens was collected and RNA was extracted. The RNA was selected for poly-A tails. Normalization by denature/renature was applied to synthesized cDNA. The cDNA were then size selected for 1kb and 2kb lengths using Ampure beads. For the 1kb cDNA, 11 SMRT cells were used. For the 2kb cDNA, 14 SMRT cells were used. Sequencing was performed on an RSII Pacific Biosciences machine using P4C2 chemistry. PacBio RS ERX1417599 ena-EXPERIMENT-ROSLIN INSTITUTE, UNIVERSITY OF EDINBURGH-01-04-2016-11:45:44:783-24 ERP014795 1kb size selected ERS1101150 SAMEA3914016 J-line Chickens Brain Isoseq 24 OTHER TRANSCRIPTOMIC other Brain tissue from J-line chickens was collected and RNA was extracted. The RNA was selected for poly-A tails. Normalization by denature/renature was applied to synthesized cDNA. The cDNA were then size selected for 1kb and 2kb lengths using Ampure beads. For the 1kb cDNA, 11 SMRT cells were used. For the 2kb cDNA, 14 SMRT cells were used. Sequencing was performed on an RSII Pacific Biosciences machine using P4C2 chemistry. PacBio RS ERX1417600 ena-EXPERIMENT-ROSLIN INSTITUTE, UNIVERSITY OF EDINBURGH-01-04-2016-11:45:44:783-25 ERP014795 1kb size selected ERS1101151 SAMEA3914017 J-line Chickens Brain Isoseq 25 OTHER TRANSCRIPTOMIC other Brain tissue from J-line chickens was collected and RNA was extracted. The RNA was selected for poly-A tails. Normalization by denature/renature was applied to synthesized cDNA. The cDNA were then size selected for 1kb and 2kb lengths using Ampure beads. For the 1kb cDNA, 11 SMRT cells were used. For the 2kb cDNA, 14 SMRT cells were used. Sequencing was performed on an RSII Pacific Biosciences machine using P4C2 chemistry. PacBio RS