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Carefully calculated haplotype frequency sets are used in conjunction with probabilistic matching algorithms. They enable the calculation of match probabilities (shown as percentages) across donor phenotypes as well as individual loci when a search is performed in WMDA’s Search & Match Service.

With the last release of our the Search & Match Service, the WMDA  introduces has maintained a new similar haplotype frequency set configuration to better serve all patients and provide increased accuracy when matching donors and cord blood units to patients. The Search & Match Service currently contains no ethnicity information for donors and therefore the new frequency sets will be calculated and based upon geographical and available data of the donors of an organisation. These frequency sets utilize high resolution typing results as was used for Optimatch (Search & Match v1). In most cases the ION of the donor/cord blood unit will determine which haplotype frequency set is used.

To provide a more up-to-date representation of the donor pools worldwide, the haplotype frequency set calculations have been performed using the latest data in the WMDA Donor and CBU database. Calculations were performed using the open source algorithm Haplo-o-Mat (https://github.com/DKMS/Hapl-o-Mat and https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5450239/and applying it to high resolution donor typing results received from listing organisations to extrapolate the possible from organisations to extrapolate the haplotypes of the region or organisation. Thus, an organisation or geographical region must meet a minimum threshold of number of donors and availability of high resolution typing both quantity and quality HLA typed records  to build usable and valuable frequencies. For cord blood units. , we will use the same sets that were determined in for the donor populations.

The inclusion criteria aims to balance a the high number of donors, the quality of the HLA types and the complexity of the haplotype frequency estimation. The number and HLA types of the loci that are included in the estimation can be independent of the loci of the haplotypes actually estimated if the quality of the former is appropriate.

5-locus Haplofrequency Locus haplotype frequency estimation was performed on all organisations/populations with at least 5000 10 000 donors in typed for HLA-A, -B, -C and -DRB1 types in 90% high resolution, -DRB1 and -DQB1 where ambiguity was low enough to be useful. Organisations in the same country /that recruit from within the same population are usually combined, e.g. AT-ABMDR (Austrian ION-2614, Austrian Bone Marrow Donors) and ATand AT-Verein GFL (Austria- Verein geben fur LebelION-4961, Verein Geben für Leben) but *not* for US-NMDP (general US population) and US-GOL (predominantly Ashkenazi Jews). The 90% criteria is based on the  

A global frequency set and includes all allele codes whose top 90% cumulated allele frequencies are in high resolution.The current global frequency set will continue to be used for donors of organisations if it is the best representationwas also calculated and will  be used for all patients and donors that, for some reason, do not match a typical haplotype frequency set. For example, when a registry is new and has not yet been assigned to an appropriate existing haplotype frequency set or when the from this registry deviate substantially enough from any typical haplotype frequency set that it does not make sense to assign them to an existing one. The number of this frequency set is 999. Information about which haplotype frequency set is applied to a donor search is provided in the search results API endpoint. 

Below, you can find a figure information on how the haplotype frequency (HF) sets are assigned to the donors and cord blood units. The system search service first determines if both COUNTRY and ETHNICITY are provided. registry ION and ethnicity of the donor or cord blood unit provided. Registry ION is then used to look up the country/region that the donor or cord blood unit belongs to. If yes, then it will check if an ethnicity specific set for this country existsregistry is assigned. If the donor, for example, is coming from USA and has ethnicity HISA, then we do not have a specific set available. However, there is a more broad Hispanic HF haplotype frequency set available (USA-HI) and this will then be used in this scenario.

If there is no ethnicity available for the donor or no ethnicity specific HF haplotype frequency set exists for that country, the system will check if a country specific HF haplotype frequency set is available or if the country is part of one of the regional HF haplotype frequency sets.

If no country specific HF haplotype frequency set is available, the Search & Match Service will use the global consensus HF haplotype frequency set.


Imagefloat
captionFlowchart assigning a haplotype frequency (HF) set

...

South America (sam): AR, BR, UY (Set number: 34)





Input Data

Applied to:

INPUT DATA

HF set number

(pop_id)

Determination date

Sample size

ISO country code

ION

Search & Match Service_Registry_codes

Old BMDW Registry codes
IONs
1
2017
2022-
04-2526,352
05226507AR5117

AR-INCUCAI

AR
Same
2
2017
2022-
04-2521,709
05149750AT

2614

4961

AT-ABMDR

AT-Verein

A

A2

Same +

8162 - AT-Vita34 (CBB)

3
2017
2022-
04-2538,548NZ
0541348AU + NZ

7748

8261

AU-ABMDR

NZ-NZBMDR

AUS

Same
4
2017
2022-
04-2549,392
0536351

BE

4201

BE-MDPB

B
Same
5
2017
2022-
04-2582,656
0581859BR8766

BR-REDOME

BR
Same
6
2017
2022-
04-25214,836
0568077CA

5103

6912

CA-One Match

CA-HemaQuec

CND

CND3

Same +

3066 - CA-VAR (CBB)

7
2017
2022-
04-2589,533
05114900CH9341

CH-SBSC

CH
Same
8
2017
2022-
04-25591,099
05564150CN + HK + TW

2197

6681

4070

3458

CN-CMDP

CN-

Sunsh

Sunshine

HK-HKBMDR

TW-

Tzu Chi

CN

CN1

HK

TW

92017-04-25

TzuChi

Same +

1212 - TW-SinoCell (CBB)

1714 - TW-Meribank (CBB)

3105 - HK-CBB (CBB)

5812 - TW-StemCyte (CBB)

6459 - TW-Bionet (CBB)

6692 - TW-Healthbanks (CBB)

9281 - HK-Mononuclear (CBB)

92022-0574633
27,230
CY

4278

9751

CY-

Par BMDR

Paraskevaidio

CY-CBMDR

CY
Same

CY2

10
2017
2022-
04-2536,878
0575810CZ

4753

5440

CZ-CSCR

CZ-CNMDR

CS

CS2
Same
11
2017
2022-
04-256,273,693
052627544DE

5525

6939

DE-DKMS

DE-ZKRD

D

Same +

DE-DUS (CBB)

All ethnicities except for ASSW
12
2017
2022-
04-2520,364
0553849DK

2015

7484

DK-DSCDW

DK-DSDE

DK
Same

DK2

13
2017
2022-
04-2559,177
0581265ES7813

ES-REDMO

E(+E2)
Same
14
2017
2022-
04-2517,377
0539567FI9738
Fi
FI-FSCR
FI
Same
15
2017
2022-
04-25173,541
0590069FR1804FR-FGM
F
Same
16
2017
2022-
04-251,050,556
05636595GB + IE

6354

1726

2731

9968

5590

GB-Anthony

GB-WBMDR

GB-BBMR

GB-DKMS

IE-IUBMR

GB

GB3

GB4

GB5

IRL

Same
17
2017
2022-
04-2538,855
05102358GR
1461

4979

GR-

CBMDP

HTO

GR2
Same
18
2017
2022-
04-25377,768
05651085IL

5239

4987

4068

IL-Hadassah

IL-Ezer Miz.

IL-SHBB

IL

IL2
Same

IL3

19
2017
2022-
04-25208,655
05530272IN

8486

2824

4131

4460

8196

4596

8486

IN-Datri

9935

IN-GeneBand

IN-MDR

IN-

BMST

ArjanVir

IN2

IN3

IN4

IN5

IN-ArjanVir

IN-Datri

IN-DKMS-BMST

Same
20
2017
2022-
04-25
05
150578
84477IT7450

IT-IBMDR

I
Same
21
2017
2022-
04-25129,272
05328557NL8139

NL-Matchis

NL
Same
22
2017
2022-
04-2520,925
0516499NO7214

NO-NBMDR

N
Same
23
2017
2022-
04-251,167,906
051464544PL

3918

5391

7414

PL-ALF

PL-Poltranspl

PL-DKMS

PL3
Same

PL5

PL6

24
2017
2022-
04-25158,284
0511029PT
7258
7358

PT-Cedace

P
Same
25
2017
2022-
04-2525,498
0597139SA
8118

1810

2107

SA-KFSHRC

SA-SSCDR

SA
Same
26
2017
2022-
04-2545,892
05184283SE5285

SE-Tobias

S
Same
27
2017
2022-
04-2562,785
0578885SG3785

SG-BMDP

Same +

4291 - SG-SCBB (CBB)

28
2017
2022-
04-2540,149
05122133TH8362

TH-TSCDR

TH
Same
29
2017
2022-
04-2532,572TRIS
05491941TR

3893

5509

3503

TR-TRAN

TR-TRIS

TR-TURKOK

TRAN

Same

TRKK

30
2017
2022-
04-254,068,326
051723292US3553

US-NMDP

USA1312017-04-25163,588

3553 with ethnicities: 

  • None provided
  • MX
  • OT
  • UK

and the following organisations (all ethnicities)

4857 - US-CSCC (CBB)

6579 - US-Cleveland (CBB)

6738 - ZA-DKMS 

7470 - US-Lifebank

8118 - ZA-SABMR

8379 - US-StemCyte (CBB)

8691 - US-NCBP (CBB) 

312022-0597953US-GOL
US
1033

US-GOL

USA4
Same
32
2017
2022-
04-25792,159
05564561East Asia: CN+HK+TW+JP

eas

Search&Match:easCN+CN1+HK+TW+JP332017-04-251,369,965342017-04-25109,841

1212

1714

2197

3105

3458

4070

5812

6459

6681

6692

6933


4364 - JP-JMDP

8405 - KR-KONOS

All other IONs that were used as input have their own country/region specific set. 

332022-052398213

Eastern Europe: AT+CZ+CY+GR+PL+TR+BG+HU+

HR+LT+MK+RU+RO+RS+SK+SI

eeuSearch&Match:eeu

A+A2+CS+CS2+CY+CY2+GR+GR2+PL3+PL5+PL6+TRAN+

TRIS+TRKK+BG+H+HR+LT+MK+R2+R4+RO+RS+SK+SLO

1005
1372
1695
2073
2614
3503
3893
3918
4278
4307
4398
4565
4650
4753
4961
4979
5019
5391
5440
5509
5712
7197
7414
8162
8256
8714
9751
9778

1005
1372
4381
4398
4565
4650
5070
5712
7197
8256
8714
9778

342022-05413438South America:

AR+BR+UY
samSearch&Match:samAR+BR+UY100
+CL+PY

1574

2547

5117

6517

8766

CL-DKMS

PY-VKS

AR-INCUCAI

UY-SINDOME

BR-REDOME

1574 - CL-DKMS

2547 - PY-VKS

4675 - CL-Vidacel (CBB)

6517 - UY-SINDOME

Brazil and Argentina have their own country-specific sets. 

352022-0538530ZA

6738

8118

ZA-DKMS

ZA-SABMR

None yet. Under investigation. 
362022-0535895IR

4993

6887

IR-INSCDN

IR-ISCDP

None yet. Under investigation. 
412022-0511012LU3099

LU-LMDP

Same
1002022-05
2016-09-30
151,204DE-ASSW
-DE-ASSW subset

5525

6939

Subset of donors from these registries with ethnicity:

  • ASSW
Same
DE-ASSW
101
2017
2022-
04-
05656,591US-AF
(ZKRD)-

US-AF subset (ZKRD_estimation)

USA1-AF
*3553

Subset of donors from this registry with ethnicities:

  • AF
  • AFNA
  • AFSS

Same

+3034

1022022-
1022017-04-
05796,780US-AS
(ZKRD)-US-AS subset (ZKRD_estimation)USA1-AS103
*3553

Subset of donors from this registry with ethnicities:

  • ASNE
  • AS
  • ASCE
  • ASOC
  • ASSE
  • ASSO
  • ASSW
Same
1032022-
2017-04-
053,740,668US-CA
(ZKRD)-US-CA subset (ZKRD_estimation)USA1-CA
*3553

Subset of donors from this registry with ethnicities:

  • CANA
  • CA
  • CAAU
  • CAER
  • CAEU
Same
1042022
1042017-04
-051,002,893US-HI
(ZKRD)-US-HI subset (ZKRD_estimation)USA1-HI
*3553

Subset of donors from this registry with ethnicities:

  • HISA
  • HI
  • HICA

Same

+ 1671

9992022-05
9992015-12-16
11,430,561
Global consensus


All donorsAll
Search & Match Service donor registries with a sufficient number of donors with the defined level of HLA typing.
donors/ CBUs not specifically matching any other set. 

In order for WMDA to perform Since WMDA is doing these calculations on behalf of member organisations, it is important for organisations to submit donor ethnicity data and high resolution typing when available and donor ethnicity data. This greatly improves the haplofrequency haplotype frequency sets generated and allows for individual donor match grades to be more accurate

NOTE: None of the Japanese and Korean donors have been typed for DQB1. This means that no Japanese or Korean donors were included in the calculations for set #32. Therefore, the haplotype frequency set applied to Japanese and Korean donors is likely to be biased against Japanese and Korean . We have kindly received a self-generated haplotype frequency set from the Japanese registry and are working on integrating it in the updated Search & Match Service. Whether to apply the provided Japanese haplotype frequency set or to apply set #32 is still under investigation. 

NOTE: in some cases, a country’s donors may be used in a national haplotype frequency set as well as a regional one. For example, Austrian donors are used in their own set (#2) as well as the Eastern Europe regional set (#33). When calculating match probabilities, the most specific set is always used. So for donors from Austrian Bone Marrow Donor Registry or Verein Geben für Leben set #2 is used, but for Slovakian donors there were not enough donors typed at high resolution to calculate their own set and so the regional set is assigned (#33)

There are also countries or donors with a specific ethnic background in a country for which there was no specific haplotype frequency set in Optimas, but for which there are now enough donors for their own haplotype frequency set and/or their haplotype. We are currently investigating whether it would provide benefit to host these separately. These include: 

  • IN-DATRI: Since DATRI is recruiting in a specific region of India, its haplotype frequencies may be significantly different from the haplotype frequencies found throughout the greater India (set #19).
  • ZA: There are enough donors from South Africa typed at high resolution to merit its own set. Considering the unique heritage of South African donors, having frequency sets per ethnic group would be especially beneficial.
It is important to know that

...

the haplotype frequency assigned to your organisation can be changed!

You can request that your donors be returned to the global consensus haplofrequency haplotype frequency set or to a regional set. Your request should include the reasons why you believe that another set is more applicable for your donors. Additionally, if your organisation has a frequency set available that you would like to see utilized for the donors of your organisation, we can implement it as well. In this case, your request should include at least a description about your population, the sample size, inclusion and exclusion criteria, calculation method, and the reasons why your haplofrequency haplotype frequency set would be better than the current set applied by WMDA. Both requests will be reviewed by the WMDA BioInformatics Bioinformatics & Innovation Working Group. Please send requests to support@wmda.info . In the future, you'll be able to dictate a frequency set on a per donor basis. 


DateVersionDescriptionAuthor
2017-10-311.0Replacement BMDW global haplotype frequency set for more specific setsJK
2018-01-241.1Modification some sets; introduced during OptiMatch version 3.31.0JK
2019-02-151.2Replaced BMDW by WMDA / Search & Match Service; updated email addressJK
2022-08-151.3Copied original page and updated with relevant info for HAP-E algorithm. MM