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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 numberTitle of the applicationFiling DateStatus
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
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