![](/images/general/no_picture/200_user.png)
Louis S Zarfas
Examiner (ID: 12140)
Most Active Art Unit | 2902 |
Art Unit(s) | 2914, 2902, 2904, 2900 |
Total Applications | 4726 |
Issued Applications | 4667 |
Pending Applications | 1 |
Abandoned Applications | 58 |
Applications
Application number | Title of the application | Filing Date | Status |
---|---|---|---|
Array
(
[id] => 16949456
[patent_doc_number] => 20210208147
[patent_country] => US
[patent_kind] => A1
[patent_issue_date] => 2021-07-08
[patent_title] => METHOD OF PROGNOSIS AND FOLLOW UP OF PRIMARY LIVER CANCER
[patent_app_type] => utility
[patent_app_number] => 16/754164
[patent_app_country] => US
[patent_app_date] => 2018-10-15
[patent_effective_date] => 0000-00-00
[patent_drawing_sheets_cnt] => 0
[patent_figures_cnt] => 0
[patent_no_of_words] => 14980
[patent_no_of_claims] => 0
[patent_no_of_ind_claims] => -23
[patent_words_short_claim] => 91
[patent_maintenance] => 1
[patent_no_of_assignments] => 0
[patent_current_assignee] =>[type] => publication
[pdf_file] =>[firstpage_image] =>[orig_patent_app_number] => 16754164
[rel_patent_id] =>[rel_patent_doc_number] =>) 16/754164 | METHOD OF PROGNOSIS AND FOLLOW UP OF PRIMARY LIVER CANCER | Oct 14, 2018 | Pending |
Array
(
[id] => 16000411
[patent_doc_number] => 20200176076
[patent_country] => US
[patent_kind] => A1
[patent_issue_date] => 2020-06-04
[patent_title] => SCANSOFT: A METHOD FOR THE DETECTION OF GENOMIC DELETIONS AND DUPLICATIONS IN MASSIVE PARALLEL SEQUENCING DATA
[patent_app_type] => utility
[patent_app_number] => 16/631644
[patent_app_country] => US
[patent_app_date] => 2018-07-09
[patent_effective_date] => 0000-00-00
[patent_drawing_sheets_cnt] => 0
[patent_figures_cnt] => 0
[patent_no_of_words] => 10001
[patent_no_of_claims] => 0
[patent_no_of_ind_claims] => -20
[patent_words_short_claim] => 20
[patent_maintenance] => 1
[patent_no_of_assignments] => 0
[patent_current_assignee] =>[type] => publication
[pdf_file] =>[firstpage_image] =>[orig_patent_app_number] => 16631644
[rel_patent_id] =>[rel_patent_doc_number] =>) 16/631644 | SCANSOFT: A METHOD FOR THE DETECTION OF GENOMIC DELETIONS AND DUPLICATIONS IN MASSIVE PARALLEL SEQUENCING DATA | Jul 8, 2018 | Pending |
Array
(
[id] => 16858155
[patent_doc_number] => 20210158900
[patent_country] => US
[patent_kind] => A1
[patent_issue_date] => 2021-05-27
[patent_title] => A METHOD AND SYSTEM FOR GENE SIGNATURE MARKER SELECTION
[patent_app_type] => utility
[patent_app_number] => 16/624526
[patent_app_country] => US
[patent_app_date] => 2018-06-25
[patent_effective_date] => 0000-00-00
[patent_drawing_sheets_cnt] => 0
[patent_figures_cnt] => 0
[patent_no_of_words] => 9434
[patent_no_of_claims] => 0
[patent_no_of_ind_claims] => -13
[patent_words_short_claim] => 395
[patent_maintenance] => 1
[patent_no_of_assignments] => 0
[patent_current_assignee] =>[type] => publication
[pdf_file] =>[firstpage_image] =>[orig_patent_app_number] => 16624526
[rel_patent_id] =>[rel_patent_doc_number] =>) 16/624526 | A METHOD AND SYSTEM FOR GENE SIGNATURE MARKER SELECTION | Jun 24, 2018 | Abandoned |
Array
(
[id] => 15969093
[patent_doc_number] => 20200168298
[patent_country] => US
[patent_kind] => A1
[patent_issue_date] => 2020-05-28
[patent_title] => GENOTYPING USING HIGH THROUGHPUT SEQUENCING DATA
[patent_app_type] => utility
[patent_app_number] => 16/615089
[patent_app_country] => US
[patent_app_date] => 2018-05-21
[patent_effective_date] => 0000-00-00
[patent_drawing_sheets_cnt] => 0
[patent_figures_cnt] => 0
[patent_no_of_words] => 22563
[patent_no_of_claims] => 0
[patent_no_of_ind_claims] => -22
[patent_words_short_claim] => 186
[patent_maintenance] => 1
[patent_no_of_assignments] => 0
[patent_current_assignee] =>[type] => publication
[pdf_file] =>[firstpage_image] =>[orig_patent_app_number] => 16615089
[rel_patent_id] =>[rel_patent_doc_number] =>) 16/615089 | GENOTYPING USING HIGH THROUGHPUT SEQUENCING DATA | May 20, 2018 | Pending |
Array
(
[id] => 15442297
[patent_doc_number] => 20200035332
[patent_country] => US
[patent_kind] => A1
[patent_issue_date] => 2020-01-30
[patent_title] => METHOD AND APPARATUS FOR MASKING CLINICALLY IRRELEVANT ANCESTRY INFORMATION IN GENETIC DATA
[patent_app_type] => utility
[patent_app_number] => 16/500459
[patent_app_country] => US
[patent_app_date] => 2018-04-04
[patent_effective_date] => 0000-00-00
[patent_drawing_sheets_cnt] => 0
[patent_figures_cnt] => 0
[patent_no_of_words] => 6177
[patent_no_of_claims] => 0
[patent_no_of_ind_claims] => -10
[patent_words_short_claim] => 112
[patent_maintenance] => 1
[patent_no_of_assignments] => 0
[patent_current_assignee] =>[type] => publication
[pdf_file] =>[firstpage_image] =>[orig_patent_app_number] => 16500459
[rel_patent_id] =>[rel_patent_doc_number] =>) 16/500459 | METHOD AND APPARATUS FOR MASKING CLINICALLY IRRELEVANT ANCESTRY INFORMATION IN GENETIC DATA | Apr 3, 2018 | Abandoned |
Array
(
[id] => 15502957
[patent_doc_number] => 20200051667
[patent_country] => US
[patent_kind] => A1
[patent_issue_date] => 2020-02-13
[patent_title] => METHOD AND SYSTEMS FOR THE EFFICIENT COMPRESSION OF GENOMIC SEQUENCE READS
[patent_app_type] => utility
[patent_app_number] => 16/485649
[patent_app_country] => US
[patent_app_date] => 2017-12-15
[patent_effective_date] => 0000-00-00
[patent_drawing_sheets_cnt] => 0
[patent_figures_cnt] => 0
[patent_no_of_words] => 21431
[patent_no_of_claims] => 0
[patent_no_of_ind_claims] => -80
[patent_words_short_claim] => 89
[patent_maintenance] => 1
[patent_no_of_assignments] => 0
[patent_current_assignee] =>[type] => publication
[pdf_file] =>[firstpage_image] =>[orig_patent_app_number] => 16485649
[rel_patent_id] =>[rel_patent_doc_number] =>) 16/485649 | METHOD AND SYSTEMS FOR THE EFFICIENT COMPRESSION OF GENOMIC SEQUENCE READS | Dec 14, 2017 | Pending |
Array
(
[id] => 14780687
[patent_doc_number] => 20190265241
[patent_country] => US
[patent_kind] => A1
[patent_issue_date] => 2019-08-29
[patent_title] => METHOD OF DIAGNOSIS OF NON-ALCOHOLIC FATTY LIVER DISEASES
[patent_app_type] => utility
[patent_app_number] => 16/333667
[patent_app_country] => US
[patent_app_date] => 2017-09-15
[patent_effective_date] => 0000-00-00
[patent_drawing_sheets_cnt] => 0
[patent_figures_cnt] => 0
[patent_no_of_words] => 11891
[patent_no_of_claims] => 0
[patent_no_of_ind_claims] => -17
[patent_words_short_claim] => 2
[patent_maintenance] => 1
[patent_no_of_assignments] => 0
[patent_current_assignee] =>[type] => publication
[pdf_file] =>[firstpage_image] =>[orig_patent_app_number] => 16333667
[rel_patent_id] =>[rel_patent_doc_number] =>) 16/333667 | METHOD OF DIAGNOSIS OF NON-ALCOHOLIC FATTY LIVER DISEASES | Sep 14, 2017 | Pending |
Array
(
[id] => 14721947
[patent_doc_number] => 20190252037
[patent_country] => US
[patent_kind] => A1
[patent_issue_date] => 2019-08-15
[patent_title] => Viral Polypeptide Fragments That Bind Cellular POL II C-Terminal Domain (CTD) and Their Uses
[patent_app_type] => utility
[patent_app_number] => 16/315882
[patent_app_country] => US
[patent_app_date] => 2017-07-07
[patent_effective_date] => 0000-00-00
[patent_drawing_sheets_cnt] => 0
[patent_figures_cnt] => 0
[patent_no_of_words] => 34317
[patent_no_of_claims] => 0
[patent_no_of_ind_claims] => -18
[patent_words_short_claim] => 24
[patent_maintenance] => 1
[patent_no_of_assignments] => 0
[patent_current_assignee] =>[type] => publication
[pdf_file] =>[firstpage_image] =>[orig_patent_app_number] => 16315882
[rel_patent_id] =>[rel_patent_doc_number] =>) 16/315882 | Viral Polypeptide Fragments That Bind Cellular POL II C-Terminal Domain (CTD) and Their Uses | Jul 6, 2017 | Pending |
Array
(
[id] => 15148475
[patent_doc_number] => 20190352715
[patent_country] => US
[patent_kind] => A1
[patent_issue_date] => 2019-11-21
[patent_title] => NON-INVASIVE DIAGNOSTIC OF NON-ALCOHOLIC STEATOHEPATITIS
[patent_app_type] => utility
[patent_app_number] => 16/089835
[patent_app_country] => US
[patent_app_date] => 2017-03-30
[patent_effective_date] => 0000-00-00
[patent_drawing_sheets_cnt] => 0
[patent_figures_cnt] => 0
[patent_no_of_words] => 20586
[patent_no_of_claims] => 0
[patent_no_of_ind_claims] => -14
[patent_words_short_claim] => 53
[patent_maintenance] => 1
[patent_no_of_assignments] => 0
[patent_current_assignee] =>[type] => publication
[pdf_file] =>[firstpage_image] =>[orig_patent_app_number] => 16089835
[rel_patent_id] =>[rel_patent_doc_number] =>) 16/089835 | NON-INVASIVE DIAGNOSTIC OF NON-ALCOHOLIC STEATOHEPATITIS | Mar 29, 2017 | Pending |
Array
(
[id] => 19258283
[patent_doc_number] => 12018329
[patent_country] => US
[patent_kind] => B2
[patent_issue_date] => 2024-06-25
[patent_title] => Diagnosing fetal chromosomal aneuploidy using massively parallel genomic sequencing
[patent_app_type] => utility
[patent_app_number] => 13/070275
[patent_app_country] => US
[patent_app_date] => 2011-03-23
[patent_effective_date] => 0000-00-00
[patent_drawing_sheets_cnt] => 20
[patent_figures_cnt] => 25
[patent_no_of_words] => 16081
[patent_no_of_claims] => 4
[patent_no_of_ind_claims] => 1
[patent_words_short_claim] => 167
[patent_maintenance] => 1
[patent_no_of_assignments] => 0
[patent_current_assignee] =>[type] => patent
[pdf_file] =>[firstpage_image] =>[orig_patent_app_number] => 13070275
[rel_patent_id] =>[rel_patent_doc_number] =>) 13/070275 | DIAGNOSING FETAL CHROMOSOMAL ANEUPLOIDY USING MASSIVELY PARALLEL GENOMIC SEQUENCING | Mar 22, 2011 | Pending |
Array
(
[id] => 6317070
[patent_doc_number] => 20100112590
[patent_country] => US
[patent_kind] => A1
[patent_issue_date] => 2010-05-06
[patent_title] => 'Diagnosing Fetal Chromosomal Aneuploidy Using Genomic Sequencing With Enrichment'
[patent_app_type] => utility
[patent_app_number] => 12/614350
[patent_app_country] => US
[patent_app_date] => 2009-11-06
[patent_effective_date] => 0000-00-00
[patent_drawing_sheets_cnt] => 21
[patent_figures_cnt] => 21
[patent_no_of_words] => 16548
[patent_no_of_claims] => 25
[patent_no_of_ind_claims] => 3
[patent_words_short_claim] => 0
[patent_maintenance] => 1
[patent_no_of_assignments] => 0
[patent_current_assignee] =>[type] => publication
[pdf_file] => publications/A1/0112/20100112590.pdf
[firstpage_image] =>[orig_patent_app_number] => 12614350
[rel_patent_id] =>[rel_patent_doc_number] =>) 12/614350 | Diagnosing Fetal Chromosomal Aneuploidy Using Genomic Sequencing With Enrichment | Nov 5, 2009 | Pending |
Array
(
[id] => 5521396
[patent_doc_number] => 20090029377
[patent_country] => US
[patent_kind] => A1
[patent_issue_date] => 2009-01-29
[patent_title] => 'DIAGNOSING FETAL CHROMOSOMAL ANEUPLOIDY USING MASSIVELY PARALLEL GENOMIC SEQUENCING'
[patent_app_type] => utility
[patent_app_number] => 12/178181
[patent_app_country] => US
[patent_app_date] => 2008-07-23
[patent_effective_date] => 0000-00-00
[patent_drawing_sheets_cnt] => 10
[patent_figures_cnt] => 10
[patent_no_of_words] => 11503
[patent_no_of_claims] => 23
[patent_no_of_ind_claims] => 3
[patent_words_short_claim] => 0
[patent_maintenance] => 1
[patent_no_of_assignments] => 0
[patent_current_assignee] =>[type] => publication
[pdf_file] => publications/A1/0029/20090029377.pdf
[firstpage_image] =>[orig_patent_app_number] => 12178181
[rel_patent_id] =>[rel_patent_doc_number] =>) 12/178181 | DIAGNOSING FETAL CHROMOSOMAL ANEUPLOIDY USING MASSIVELY PARALLEL GENOMIC SEQUENCING | Jul 22, 2008 | Pending |