We are the next generation:

Sequencing Services

Our Services

Genome
Sequencing

Know it all. Using a single approach to learn the entire genetic background of an individual.

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Exome
Sequencing

Focused. Whole-exome sequencing screens protein-coding regions of the genome to uncover genetic influences on diseases.

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Targeted
Sequencing

Deep dive. Panel Sequencing allows a very distinct and therefore very deep view on gene alterations. Even small clones do not escape.

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RNA
Sequencing

All things RNA. The expression of the transcriptome provides the basis for the identity of a cell and the associated functionality.

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Single-cell
Sequencing

Diversity. Single-cell sequencing captures the diversity of a sample by measuring thousands of individual cells simulteanously.

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Methylation
Sequencing

The level above. Epigenetic analyses allow insight to a higher level regulation of gene expression and chromatin remodelling.

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Sequencing
only

The one and only. The desired number of clusters or output determine the sequencing of the ready-to-load library.

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Data
Analysis

Exploration. Large data sets want to be analyzed and made accessible to the user.

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Data
Visualization

Show and tell. Visualization facilitates interpretation and generation of hypotheses. A picture says more than four letters.

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»Our Vision is to understand the genetic and molecular basics of diseases in all their complexity and to use that knowledge to refine the diagnostic and therapeutic possibilities for every patient.«

Prof. Dr. med. Dr. phil. Torsten Haferlach Managing Partner

About us

5,000 genomes


The 5k project
strengthened our expertise to sequence at the most qualitative level in high throughput with shortest turn-around times in a clinical setting.

mll.com

News

Integrated DNA Technologies Adds MLL Munich Leukemia Laboratory to Align Program

News Release - 21 March 2022

News Release

MLL Dx Successfully Accredited by the College of American Pathologists (CAP)

News - July 2021

Certificate

Find more news on publications and references

News

Publications/References

Realising the potential of WTS

other reports and publications

Leukaemia diagnosis: Realising the potential of whole transcriptome sequencing. Research Features. Health & Medicine. Walter W. March 10th 2022.

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Analytical demands to use WGS

peer-reviewed

Analytical Demands to Use Whole-Genome Sequencing in Precision Oncology. Meggendorfer M et al.  Semin Cancer Biol. 2021 Jun 10;S1044-579X(21)00179-6. Online ahead of print.

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Next-generation diagnostics

peer-reviewed

Next-generation diagnostics for precision oncology: Preanalytical considerations, technical challenges, and available technologies. Walter et al. Semin Cancer Biol. 2020 Nov 7;S1044-579X(20)30220-0.

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WGS and WTS a new tool?

peer-reviewed

WGS and WTS in leukaemia: A tool for diagnostics? Meggendorfer M et al. Best Pract Res Clin Haematol. 2020 Sep;33(3):101190.

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Large-scale sequencing

scientific report

Large-scale sequencing experience from the MLL 5K project. Walter W

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Data Visualization

scientific report

Genomic & Transcriptomic Data Visualization. Walter W

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Find more publications and references on

Publications