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SEQHLA FOR THE ANALYSIS OF YOUR
HLA SANGER SEQUENCING DATA

NO CLOUD - STAY IN CONTROL OF YOUR DATA

SEQHLA

SEQHLA is a powerful and user-friendly application for the analysis of HLA sequence based typing data from all Sanger sequencing platforms. All IMGT HLA database versions are available for download and import. It uses an unique learning base caller based on peak area statistic data and has its own auto edit function.

Constant positions can be ignored for analysis if desired. The result can be displayed in maximum, 1 field or 2 field resolution and as NMPD code. All result data can be transferred to laboratory internal LIM Systems and / or issued as personalised patient reports.

  • HIGHLIGHTS

    • Compatible with data from all common Sanger sequencing platforms and kits
    • Easy setup of individual target regions based on the IMGT HLA database
    • Configurable base caller with sequencer dependent thresholds
    • Automatic and user defined trimming of sequencing result files
    • All results for one patient shown in one screen incl. detected allele combinations
    • Automatic warning for splice site mutations
    • Possibility of ignoring constant positions for the analysis

     

     

     

    • Detection of new alleles
    • Display of results in different resolutions (1 field, 2-field, and max. resolution) and as NMDP code
    • Peak area statistic: an automatic comparison to all previously analysed samples for a sensitive detection of heterozygous positions even in case of an allelic dropout
    • Detailed HLA report for individual patients / orders
    • Data import (LISTENMASTER) / export (TALKMASTER) from / to any LIM System

     
  • Compatible with data from all common Sanger sequencing platforms and kits
  • Easy setup of individual target regions based on the IMGT HLA database
  • Configurable base caller with sequencer dependent thresholds
  • Automatic and user defined trimming of sequencing result files
  • All results for one patient shown in one screen incl. detected allele combinations
  • Automatic warning for splice site mutations
  • Possibility of ignoring constant positions for the analysis

 

  • Detection of new alleles
  • Display of results in different resolutions (1 field, 2-field, and max. resolution) and as NMDP code
  • Peak area statistic: an automatic comparison to all previously analysed samples for a sensitive detection of heterozygous positions even in case of an allelic dropout
  • Detailed HLA report for individual patients / orders
  • Data import (LISTENMASTER) / export (TALKMASTER) from / to any LIM System