b'Bioinformatics Software Next-Generation Sequencing (NGS) | RUO AssaysSequencing SummaryUsing the merged read summary interpretation is quick and easy.1 Easy identification of specific types of gene rearrangements such as IGHV3-21.Merge% TotalCumulative Mutation rate In-frameNo stop Rank Sequence Length count V-gene J-gene reads %partial V-gene(Y/N) codon V-coverage(%) (Y/N)1 TTCTCGTGGTG 455 29603 IGHV4-59_08 IGHJ4_02 9.93 9.93 11.26 Y Y 98.632 CTCGCCCTCCT 463 205 IGHV5-51_01 IGHJ4_02 0.07 9.99 0.00 Y Y 99.663 GGTTTTCCTTG 484 201 IGHV3-7_01 IGHJ4_02 0.07 10.06 7.77 Y Y 100.004 CTCGCCCTCCT 463 185 IGHV5-51_01 IGHJ5_02 0.06 10.12 6.08 Y Y 99.325 CTCGCCCTCCT 469 170 IGHV5-51_01 IGHJ4_02 0.06 10.18 0.00 Y Y 99.326 CTCGCCCTCCT 466 160 IGHV5-51_01 IGHJ4_02 0.05 10.23 0.00 Y Y 99.667 CTGCTGCTGAC 460 159 IGHV2-5_10 IGHJ5_02 0.05 10.29 8.08 Y Y 97.648 GGTTTTCCTTG 493 156 IGHV3-48_02 IGHJ6_02 0.05 10.34 3.72 Y Y 98.999 CTCGCCCTCCT 334 153 IGHV5-51_02 IGHJ2_01 0.05 10.39 3.72 Y N 27.7010 CTCGCCCTCCT 334 152 IGHV5-51_02 IGHJ2_01 0.05 10.44 3.38 Y N 26.012 Identification of clonal sequences for follow upSHM rate and indicators to determine tracking with LymphoTrack MRD Software. 3 whether a clone is productive.Only provided for IGHV Leader and IGH FR1. The read summary provides sequences from a sample ranked from most abundant to least prevalent. The total read count for individual sequences is provided and no independent analysis is required to determine V and J gene families and predictions for SHM when analyzing data from LymphoTrack IGHV Leader or IGH FR1 Assays. Additionally, the software provides raw and merged data in which reads that differ by 1-2 bp are automatically merged to account for possible sequencing errors and to improve the accuracy and ease of sample interpretation. combined.Ordering InformationCatalog # Products Quantity Components7-500-0009 LymphoTrack Software- MiSeq 1 CD complimentary with kit purchase7-500-0007 LymphoTrack Software - S5/PGM 1 CD complimentary with kit purchaseInvivoscribe 2020|49'